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dbVar

Database of genomic structural variation

nsv6079590

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: 111 SVs from 19 studies. See in: genome view

Submitted genomic89,339,647-89,339,647

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6079590	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	89,339,647	89,339,647
nsv6079590	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	90,049,366	90,049,366

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17565563	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17565563	Submitted genomic		NC_000006.12:g.893 39647_89339648ins8 2	GRCh38 (hg38)		NC_000006.12	Chr6	89,339,647	89,339,647
nssv17565563	Remapped	Perfect	NC_000006.11:g.900 49366_90049367ins8 2	GRCh37.p13	First Pass	NC_000006.11	Chr6	90,049,366	90,049,366

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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