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dbVar

Database of genomic structural variation

nsv6111938

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

Submitted genomic41,643,424-41,643,424

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6111938	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	41,643,424	41,643,424
nsv6111938	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	42,039,428	42,039,428

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17642407	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17642407	Submitted genomic		NC_000022.11:g.416 43424_41643425ins2 466	GRCh38 (hg38)		NC_000022.11	Chr22	41,643,424	41,643,424
nssv17642407	Remapped	Perfect	NC_000022.10:g.420 39428_42039429ins2 466	GRCh37.p13	First Pass	NC_000022.10	Chr22	42,039,428	42,039,428

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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