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dbVar

Database of genomic structural variation

nsv5577780

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:81

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: 145 SVs from 43 studies. See in: genome view

Submitted genomic23,810,422-23,810,502

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5577780	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	23,810,422	23,810,502
nsv5577780	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	23,850,041	23,850,121

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17155107	deletion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17155107	Submitted genomic		NC_000007.14:g.238 10422_23810502delA	GRCh38 (hg38)		NC_000007.14	Chr7	23,810,422	23,810,502
nssv17155107	Remapped	Perfect	NC_000007.13:g.238 50041_23850121delA	GRCh37.p13	First Pass	NC_000007.13	Chr7	23,850,041	23,850,121

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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