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dbVar

Database of genomic structural variation

nsv5669579

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: 209 SVs from 21 studies. See in: genome view

Submitted genomic45,555,009-45,555,009

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5669579	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000022.11	Chr22	45,555,009	45,555,009
nsv5669579	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000022.10	Chr22	45,950,889	45,950,889

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17138815	insertion	HG02587	Sequencing	Sequence alignment	2,330

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17138815	Submitted genomic		NC_000022.11:g.455 55009_45555010ins9 7	GRCh38 (hg38)		NC_000022.11	Chr22	45,555,009	45,555,009
nssv17138815	Remapped	Perfect	NC_000022.10:g.459 50889_45950890ins9 7	GRCh37.p13	First Pass	NC_000022.10	Chr22	45,950,889	45,950,889

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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