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dbVar

Database of genomic structural variation

nsv5593108

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:93

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: 114 SVs from 30 studies. See in: genome view

Submitted genomic9,273,966-9,274,058

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5593108	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	9,273,966	9,274,058
nsv5593108	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	9,315,929	9,316,021

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17071548	deletion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17071548	Submitted genomic		NC_000010.11:g.927 3966_9274058delA	GRCh38 (hg38)		NC_000010.11	Chr10	9,273,966	9,274,058
nssv17071548	Remapped	Perfect	NC_000010.10:g.931 5929_9316021delA	GRCh37.p13	First Pass	NC_000010.10	Chr10	9,315,929	9,316,021

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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