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dbVar

Database of genomic structural variation

nsv5571560

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:108

Publication(s):Ebert 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: 347 SVs from 50 studies. See in: genome view

Submitted genomic1,481,630-1,481,737

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5571560	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	1,481,630	1,481,737
nsv5571560	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	1,521,266	1,521,373

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17144435	deletion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17144435	Submitted genomic		NC_000007.14:g.148 1630_1481737delA	GRCh38 (hg38)		NC_000007.14	Chr7	1,481,630	1,481,737
nssv17144435	Remapped	Perfect	NC_000007.13:g.152 1266_1521373delA	GRCh37.p13	First Pass	NC_000007.13	Chr7	1,521,266	1,521,373

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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