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dbVar

Database of genomic structural variation

nsv5659269

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

Submitted genomic89,929,031-89,929,031

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659269	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	89,929,031	89,929,031
nsv5659269	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	90,395,375	90,395,375

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17087032	insertion	SAMN00249890	Sequencing	Sequence alignment	1,169

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17087032	Submitted genomic		NC_000014.9:g.8992 9031_89929032ins51	GRCh38 (hg38)		NC_000014.9	Chr14	89,929,031	89,929,031
nssv17087032	Remapped	Perfect	NC_000014.8:g.9039 5375_90395376ins51	GRCh37.p13	First Pass	NC_000014.8	Chr14	90,395,375	90,395,375

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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