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dbVar

Database of genomic structural variation

nsv5902244

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:8,850,407

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: 27495 SVs from 131 studies. See in: genome view

Submitted genomic156,014,074-164,864,480

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5902244	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	156,014,074	164,864,480
nsv5902244	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	156,935,226	165,785,632

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17418421	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17418421	Submitted genomic		NC_000004.12:g.156 014074_164864480de l	GRCh38 (hg38)		NC_000004.12	Chr4	156,014,074	164,864,480
nssv17418421	Remapped	Perfect	NC_000004.11:g.156 935226_165785632de l	GRCh37.p13	First Pass	NC_000004.11	Chr4	156,935,226	165,785,632

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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