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dbVar

Database of genomic structural variation

nsv5668956

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: 127 SVs from 25 studies. See in: genome view

Submitted genomic45,879,213-45,879,213

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5668956	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	45,879,213	45,879,213
nsv5668956	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	44,507,852	44,507,852

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116682	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17116682	Submitted genomic		NC_000020.11:g.458 79213_45879214ins1 51	GRCh38 (hg38)		NC_000020.11	Chr20	45,879,213	45,879,213
nssv17116682	Remapped	Perfect	NC_000020.10:g.445 07852_44507853ins1 51	GRCh37.p13	First Pass	NC_000020.10	Chr20	44,507,852	44,507,852

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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