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dbVar

Database of genomic structural variation

nsv6052653

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: 106 SVs from 23 studies. See in: genome view

Submitted genomic37,629,486-37,629,486

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6052653	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	37,629,486	37,629,486
nsv6052653	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	38,095,158	38,095,158

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17528844	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17528844	Submitted genomic		NC_000001.11:g.376 29486_37629487ins2 361	GRCh38 (hg38)		NC_000001.11	Chr1	37,629,486	37,629,486
nssv17528844	Remapped	Perfect	NC_000001.10:g.380 95158_38095159ins2 361	GRCh37.p13	First Pass	NC_000001.10	Chr1	38,095,158	38,095,158

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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