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dbVar

Database of genomic structural variation

nsv5598113

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:92

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: 146 SVs from 26 studies. See in: genome view

Submitted genomic35,906,443-35,906,534

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5598113	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	35,906,443	35,906,534
nsv5598113	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	34,494,365	34,494,456

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116870	deletion	SAMN00006580	Sequencing	Sequence alignment	9,409

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17116870	Submitted genomic		NC_000020.11:g.359 06443_35906534delA	GRCh38 (hg38)		NC_000020.11	Chr20	35,906,443	35,906,534
nssv17116870	Remapped	Perfect	NC_000020.10:g.344 94365_34494456delA	GRCh37.p13	First Pass	NC_000020.10	Chr20	34,494,365	34,494,456

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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