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dbVar

Database of genomic structural variation

nsv6112627

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: 123 SVs from 33 studies. See in: genome view

Submitted genomic21,457,394-21,457,394

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112627	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	21,457,394	21,457,394
nsv6112627	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	21,640,196	21,640,196

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17629406	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17629406	Submitted genomic		NC_000019.10:g.214 57394_21457395ins1 67	GRCh38 (hg38)		NC_000019.10	Chr19	21,457,394	21,457,394
nssv17629406	Remapped	Perfect	NC_000019.9:g.2164 0196_21640197ins16 7	GRCh37.p13	First Pass	NC_000019.9	Chr19	21,640,196	21,640,196

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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