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dbVar

Database of genomic structural variation

nsv6112630

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: 100 SVs from 20 studies. See in: genome view

Submitted genomic12,120,802-12,120,802

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112630	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	12,120,802	12,120,802
nsv6112630	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	12,231,617	12,231,617

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17632163	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17632163	Submitted genomic		NC_000019.10:g.121 20802_12120803ins2 87	GRCh38 (hg38)		NC_000019.10	Chr19	12,120,802	12,120,802
nssv17632163	Remapped	Perfect	NC_000019.9:g.1223 1617_12231618ins28 7	GRCh37.p13	First Pass	NC_000019.9	Chr19	12,231,617	12,231,617

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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