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dbVar

Database of genomic structural variation

nsv5631688

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: 76 SVs from 15 studies. See in: genome view

Submitted genomic38,018,937-38,018,937

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5631688	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	38,018,937	38,018,937
nsv5631688	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	38,307,865	38,307,865

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17070186	insertion	SAMN00000419	Sequencing	Sequence alignment	1,071

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17070186	Submitted genomic		NC_000010.11:g.380 18937_38018938ins5 29	GRCh38 (hg38)		NC_000010.11	Chr10	38,018,937	38,018,937
nssv17070186	Remapped	Perfect	NC_000010.10:g.383 07865_38307866ins5 29	GRCh37.p13	First Pass	NC_000010.10	Chr10	38,307,865	38,307,865

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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