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dbVar

Database of genomic structural variation

nsv6112623

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: 118 SVs from 29 studies. See in: genome view

Submitted genomic61,689,217-61,689,217

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112623	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	61,689,217	61,689,217
nsv6112623	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	60,264,273	60,264,273

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17622420	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17622420	Submitted genomic		NC_000020.11:g.616 89217_61689218ins1 50	GRCh38 (hg38)		NC_000020.11	Chr20	61,689,217	61,689,217
nssv17622420	Remapped	Perfect	NC_000020.10:g.602 64273_60264274ins1 50	GRCh37.p13	First Pass	NC_000020.10	Chr20	60,264,273	60,264,273

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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