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dbVar

Database of genomic structural variation

nsv5661680

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: 195 SVs from 36 studies. See in: genome view

Submitted genomic74,894,107-74,894,107

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661680	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	74,894,107	74,894,107
nsv5661680	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	75,186,448	75,186,448

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17098681	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17098681	Submitted genomic		NC_000015.10:g.748 94107_74894108ins6 7	GRCh38 (hg38)		NC_000015.10	Chr15	74,894,107	74,894,107
nssv17098681	Remapped	Perfect	NC_000015.9:g.7518 6448_75186449ins67	GRCh37.p13	First Pass	NC_000015.9	Chr15	75,186,448	75,186,448

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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