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dbVar

Database of genomic structural variation

nsv5626954

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

Submitted genomic26,556,434-26,556,434

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5626954	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000008.11	Chr8	26,556,434	26,556,434
nsv5626954	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000008.10	Chr8	26,413,950	26,413,950

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17157371	insertion	SAMN00007882	Sequencing	Sequence alignment	1,354

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17157371	Submitted genomic		NC_000008.11:g.265 56434_26556435ins4 36	GRCh38 (hg38)		NC_000008.11	Chr8	26,556,434	26,556,434
nssv17157371	Remapped	Perfect	NC_000008.10:g.264 13950_26413951ins4 36	GRCh37.p13	First Pass	NC_000008.10	Chr8	26,413,950	26,413,950

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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