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dbVar

Database of genomic structural variation

nsv4756834

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Quan et al. 2021

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: 463 SVs from 41 studies. See in: genome view

Remapped(Score: Perfect):46,144,362-46,144,362

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4756834	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000021.9	Chr21	46,144,362	46,144,362
nsv4756834	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187626.1	Chr21\|NT_1 87626.1	3,421	3,421
nsv4756834	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000021.8	Chr21	47,564,276	47,564,276

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16296545	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16296545	Remapped	Perfect	NT_187626.1:g.3421 _3422ins625	GRCh38.p12	Second Pass	NT_187626.1	Chr21\|NT_1 87626.1	3,421	3,421
nssv16296545	Remapped	Perfect	NC_000021.9:g.4614 4362_46144363ins62 5	GRCh38.p12	First Pass	NC_000021.9	Chr21	46,144,362	46,144,362
nssv16296545	Submitted genomic		NC_000021.8:g.4756 4276_47564277ins62 5	GRCh37 (hg19)		NC_000021.8	Chr21	47,564,276	47,564,276

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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