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dbVar

Database of genomic structural variation

nsv6070742

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: 105 SVs from 25 studies. See in: genome view

Submitted genomic30,183,383-30,183,383

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6070742	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	30,183,383	30,183,383
nsv6070742	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	30,151,160	30,151,160

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17562812	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17562812	Submitted genomic		NC_000006.12:g.301 83383_30183384ins1 421	GRCh38 (hg38)		NC_000006.12	Chr6	30,183,383	30,183,383
nssv17562812	Remapped	Perfect	NC_000006.11:g.301 51160_30151161ins1 421	GRCh37.p13	First Pass	NC_000006.11	Chr6	30,151,160	30,151,160

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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