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dbVar

Database of genomic structural variation

nsv5657863

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: 185 SVs from 34 studies. See in: genome view

Submitted genomic75,686,044-75,686,044

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5657863	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	75,686,044	75,686,044
nsv5657863	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	75,978,385	75,978,385

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17083897	insertion	SAMN00007703	Sequencing	Sequence alignment	1,054

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17083897	Submitted genomic		NC_000015.10:g.756 86044_75686045ins1 41	GRCh38 (hg38)		NC_000015.10	Chr15	75,686,044	75,686,044
nssv17083897	Remapped	Perfect	NC_000015.9:g.7597 8385_75978386ins14 1	GRCh37.p13	First Pass	NC_000015.9	Chr15	75,978,385	75,978,385

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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