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dbVar

Database of genomic structural variation

nsv5628286

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: 123 SVs from 31 studies. See in: genome view

Submitted genomic83,888,036-83,888,036

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5628286	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	83,888,036	83,888,036
nsv5628286	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	86,502,951	86,502,951

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17163064	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17163064	Submitted genomic		NC_000009.12:g.838 88036_83888037ins5 90	GRCh38 (hg38)		NC_000009.12	Chr9	83,888,036	83,888,036
nssv17163064	Remapped	Perfect	NC_000009.11:g.865 02951_86502952ins5 90	GRCh37.p13	First Pass	NC_000009.11	Chr9	86,502,951	86,502,951

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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