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dbVar

Database of genomic structural variation

nsv5669765

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: 221 SVs from 44 studies. See in: genome view

Submitted genomic63,669,874-63,669,874

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5669765	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	63,669,874	63,669,874
nsv5669765	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	62,301,227	62,301,227

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17119178	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
nssv17119178	Submitted genomic		NC_000020.11:g.636 69874_63669875ins1 16	GRCh38 (hg38)		NC_000020.11	Chr20	63,669,874	63,669,874
nssv17119178	Remapped	Perfect	NC_000020.10:g.623 01227_62301228ins1 16	GRCh37.p13	First Pass	NC_000020.10	Chr20	62,301,227	62,301,227

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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