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dbVar

Database of genomic structural variation

nsv5660841

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: 95 SVs from 22 studies. See in: genome view

Submitted genomic81,491,929-81,491,929

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5660841	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	81,491,929	81,491,929
nsv5660841	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	81,958,273	81,958,273

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17088620	insertion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17088620	Submitted genomic		NC_000014.9:g.8149 1929_81491930ins34 8	GRCh38 (hg38)		NC_000014.9	Chr14	81,491,929	81,491,929
nssv17088620	Remapped	Perfect	NC_000014.8:g.8195 8273_81958274ins34 8	GRCh37.p13	First Pass	NC_000014.8	Chr14	81,958,273	81,958,273

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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