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dbVar

Database of genomic structural variation

nsv6112624

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: 344 SVs from 27 studies. See in: genome view

Submitted genomic45,224,516-45,224,516

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6112624	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000021.9	Chr21	45,224,516	45,224,516
nsv6112624	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000021.8	Chr21	46,644,431	46,644,431

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17638458	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17638458	Submitted genomic		NC_000021.9:g.4522 4516_45224517ins79	GRCh38 (hg38)		NC_000021.9	Chr21	45,224,516	45,224,516
nssv17638458	Remapped	Perfect	NC_000021.8:g.4664 4431_46644432ins79	GRCh37.p13	First Pass	NC_000021.8	Chr21	46,644,431	46,644,431

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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