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dbVar

Database of genomic structural variation

nsv6015509

Organism: Homo sapiens

Study:nstd212 (Wu 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:231

Publication(s):Wu 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: 135 SVs from 33 studies. See in: genome view

Submitted genomic111,641,130-111,641,360

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6015509	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	111,641,130	111,641,360
nsv6015509	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	114,403,410	114,403,640

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17579387	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17579387	Submitted genomic		NC_000009.12:g.111 641130_111641360de l	GRCh38 (hg38)		NC_000009.12	Chr9	111,641,130	111,641,360
nssv17579387	Remapped	Perfect	NC_000009.11:g.114 403410_114403640de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	114,403,410	114,403,640

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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