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dbVar

Database of genomic structural variation

nsv4382575

Organism: Homo sapiens

Study:nstd173 (Zarrei et al. 2019)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37 (hg19)

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:33,043,324

Publication(s):Zarrei et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 104406 SVs from 146 studies. See in: genome view

Remapped(Score: Good):13,634,137-46,677,460

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv4382575	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	13,634,137	46,677,460
nsv4382575	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	15,006,458	48,097,372

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv15633274	copy number variation	11-0016-004	SNP array	Genotyping	19
nssv15658093	copy number variation	3-0608-000	SNP array	Genotyping	15

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv15633274	Remapped	Good	GRCh38.p12	First Pass	NC_000021.9	Chr21	13,634,137	46,677,460
nssv15658093	Remapped	Good	GRCh38.p12	First Pass	NC_000021.9	Chr21	13,634,137	46,677,460
nssv15633274	Submitted genomic		GRCh37 (hg19)		NC_000021.8	Chr21	15,006,458	48,097,372
nssv15658093	Submitted genomic		GRCh37 (hg19)		NC_000021.8	Chr21	15,006,458	48,097,372

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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