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dbVar

Database of genomic structural variation

nsv6067126

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: 246 SVs from 26 studies. See in: genome view

Submitted genomic22,021,592-22,021,592

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6067126	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	22,021,592	22,021,592
nsv6067126	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	21,879,103	21,879,103

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17562809	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17562809	Submitted genomic		NC_000008.11:g.220 21592_22021593ins2 760	GRCh38 (hg38)		NC_000008.11	Chr8	22,021,592	22,021,592
nssv17562809	Remapped	Perfect	NC_000008.10:g.218 79103_21879104ins2 760	GRCh37.p13	First Pass	NC_000008.10	Chr8	21,879,103	21,879,103

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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