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dbVar

Database of genomic structural variation

nsv5628199

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: 114 SVs from 28 studies. See in: genome view

Submitted genomic122,867,905-122,867,905

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5628199	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	122,867,905	122,867,905
nsv5628199	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	125,630,184	125,630,184

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17159903	insertion	HG03683	Sequencing	Sequence alignment	2,232

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17159903	Submitted genomic		NC_000009.12:g.122 867905_122867906in s177	GRCh38 (hg38)		NC_000009.12	Chr9	122,867,905	122,867,905
nssv17159903	Remapped	Perfect	NC_000009.11:g.125 630184_125630185in s177	GRCh37.p13	First Pass	NC_000009.11	Chr9	125,630,184	125,630,184

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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