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dbVar

Database of genomic structural variation

nsv5912265

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:54

Publication(s):Almarri et al. 2020

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: 228 SVs from 32 studies. See in: genome view

Submitted genomic144,581,994-144,582,047

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5912265	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	144,581,994	144,582,047
nsv5912265	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	145,807,378	145,807,431

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437864	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437864	Submitted genomic		NC_000008.11:g.144 581994_144582047de l	GRCh38 (hg38)		NC_000008.11	Chr8	144,581,994	144,582,047
nssv17437864	Remapped	Perfect	NC_000008.10:g.145 807378_145807431de l	GRCh37.p13	First Pass	NC_000008.10	Chr8	145,807,378	145,807,431

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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