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dbVar

Database of genomic structural variation

nsv5658237

Organism: Homo sapiens

Study:nstd207 (Ebert 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):Ebert 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: 258 SVs from 41 studies. See in: genome view

Submitted genomic81,426,333-81,426,333

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5658237	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	81,426,333	81,426,333
nsv5658237	Remapped	Perfect	GRCh37.p13	PATCHES	First Pass	NW_003871087.1	Chr17\|NW_0 03871087.1	80,971	80,971

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17090190	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17090190	Submitted genomic		NC_000017.11:g.814 26333_81426334ins5 7	GRCh38 (hg38)		NC_000017.11	Chr17	81,426,333	81,426,333
nssv17090190	Remapped	Perfect	NW_003871087.1:g.8 0971_80972ins57	GRCh37.p13	First Pass	NW_003871087.1	Chr17\|NW_0 03871087.1	80,971	80,971

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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