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dbVar

Database of genomic structural variation

nsv6095287

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

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

Submitted genomic112,895,808-112,895,808

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6095287	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	112,895,808	112,895,808
nsv6095287	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	115,658,088	115,658,088

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17585236	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17585236	Submitted genomic		NC_000009.12:g.112 895808_112895809in s221	GRCh38 (hg38)		NC_000009.12	Chr9	112,895,808	112,895,808
nssv17585236	Remapped	Perfect	NC_000009.11:g.115 658088_115658089in s221	GRCh37.p13	First Pass	NC_000009.11	Chr9	115,658,088	115,658,088

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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