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dbVar

Database of genomic structural variation

nsv5670003

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: 99 SVs from 14 studies. See in: genome view

Submitted genomic20,689,899-20,689,899

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5670003	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	20,689,899	20,689,899
nsv5670003	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	20,670,543	20,670,543

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116243	insertion	SAMN00000485	Sequencing	Sequence alignment	1,404

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17116243	Submitted genomic		NC_000020.11:g.206 89899_20689900ins6 977	GRCh38 (hg38)		NC_000020.11	Chr20	20,689,899	20,689,899
nssv17116243	Remapped	Perfect	NC_000020.10:g.206 70543_20670544ins6 977	GRCh37.p13	First Pass	NC_000020.10	Chr20	20,670,543	20,670,543

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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