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dbVar

Database of genomic structural variation

nsv5623000

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: 406 SVs from 24 studies. See in: genome view

Submitted genomic84,150,794-84,150,794

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5623000	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	84,150,794	84,150,794
nsv5623000	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	83,405,802	83,405,802

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17168691	insertion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17168691	Submitted genomic		NC_000023.11:g.841 50794_84150795ins8 5	GRCh38 (hg38)		NC_000023.11	ChrX	84,150,794	84,150,794
nssv17168691	Remapped	Perfect	NC_000023.10:g.834 05802_83405803ins8 5	GRCh37.p13	First Pass	NC_000023.10	ChrX	83,405,802	83,405,802

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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