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dbVar

Database of genomic structural variation

nsv5617037

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

Submitted genomic65,772,967-65,772,967

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5617037	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	65,772,967	65,772,967
nsv5617037	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	64,992,809	64,992,809

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17168259	insertion	SAMN00007703	Sequencing	Sequence alignment	1,054

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17168259	Submitted genomic		NC_000023.11:g.657 72967_65772968ins1 05	GRCh38 (hg38)		NC_000023.11	ChrX	65,772,967	65,772,967
nssv17168259	Remapped	Perfect	NC_000023.10:g.649 92809_64992810ins1 05	GRCh37.p13	First Pass	NC_000023.10	ChrX	64,992,809	64,992,809

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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