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dbVar

Database of genomic structural variation

nsv6086353

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: 177 SVs from 47 studies. See in: genome view

Submitted genomic128,118,875-128,118,875

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6086353	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	128,118,875	128,118,875
nsv6086353	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	130,881,154	130,881,154

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17579942	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17579942	Submitted genomic		NC_000009.12:g.128 118875_128118876in s85	GRCh38 (hg38)		NC_000009.12	Chr9	128,118,875	128,118,875
nssv17579942	Remapped	Perfect	NC_000009.11:g.130 881154_130881155in s85	GRCh37.p13	First Pass	NC_000009.11	Chr9	130,881,154	130,881,154

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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