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dbVar

Database of genomic structural variation

nsv5663565

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: 200 SVs from 38 studies. See in: genome view

Submitted genomic82,586,449-82,586,449

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5663565	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	82,586,449	82,586,449
nsv5663565	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	80,544,325	80,544,325

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17089073	insertion	HG01505	Sequencing	Sequence alignment	1,109

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17089073	Submitted genomic		NC_000017.11:g.825 86449_82586450ins1 7259	GRCh38 (hg38)		NC_000017.11	Chr17	82,586,449	82,586,449
nssv17089073	Remapped	Perfect	NC_000017.10:g.805 44325_80544326ins1 7259	GRCh37.p13	First Pass	NC_000017.10	Chr17	80,544,325	80,544,325

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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