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dbVar

Database of genomic structural variation

nsv5666488

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: 178 SVs from 40 studies. See in: genome view

Submitted genomic26,205,782-26,205,782

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5666488	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	26,205,782	26,205,782
nsv5666488	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	26,186,418	26,186,418

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17116157	insertion	HG00512	Sequencing	Sequence alignment	6,637

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17116157	Submitted genomic		NC_000020.11:g.262 05782_26205783ins7 3	GRCh38 (hg38)		NC_000020.11	Chr20	26,205,782	26,205,782
nssv17116157	Remapped	Perfect	NC_000020.10:g.261 86418_26186419ins7 3	GRCh37.p13	First Pass	NC_000020.10	Chr20	26,186,418	26,186,418

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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