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dbVar

Database of genomic structural variation

nsv5657830

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: 81 SVs from 23 studies. See in: genome view

Submitted genomic20,325,775-20,325,775

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657830	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	20,325,775	20,325,775
nsv5657830	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	20,793,934	20,793,934

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17085345	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
nssv17085345	Submitted genomic		NC_000014.9:g.2032 5775_20325776ins33 2	GRCh38 (hg38)		NC_000014.9	Chr14	20,325,775	20,325,775
nssv17085345	Remapped	Perfect	NC_000014.8:g.2079 3934_20793935ins33 2	GRCh37.p13	First Pass	NC_000014.8	Chr14	20,793,934	20,793,934

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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