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dbVar

Database of genomic structural variation

nsv5602679

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:58

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: 134 SVs from 36 studies. See in: genome view

Submitted genomic111,791,752-111,791,809

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5602679	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	111,791,752	111,791,809
nsv5602679	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	114,554,032	114,554,089

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17159623	deletion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17159623	Submitted genomic		NC_000009.12:g.111 791752_111791809de lG	GRCh38 (hg38)		NC_000009.12	Chr9	111,791,752	111,791,809
nssv17159623	Remapped	Perfect	NC_000009.11:g.114 554032_114554089de lG	GRCh37.p13	First Pass	NC_000009.11	Chr9	114,554,032	114,554,089

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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