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dbVar

Database of genomic structural variation

nsv5661537

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

Submitted genomic5,323,752-5,323,752

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661537	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	5,323,752	5,323,752
nsv5661537	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	5,227,047	5,227,047

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17092643	insertion	HG03125	Sequencing	Sequence alignment	5,031

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17092643	Submitted genomic		NC_000017.11:g.532 3752_5323753ins59	GRCh38 (hg38)		NC_000017.11	Chr17	5,323,752	5,323,752
nssv17092643	Remapped	Perfect	NC_000017.10:g.522 7047_5227048ins59	GRCh37.p13	First Pass	NC_000017.10	Chr17	5,227,047	5,227,047

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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