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dbVar

Database of genomic structural variation

nsv5661131

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: 121 SVs from 33 studies. See in: genome view

Submitted genomic120,852,816-120,852,816

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661131	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	120,852,816	120,852,816
nsv5661131	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	121,290,619	121,290,619

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17077488	insertion	SAMN00801888	Sequencing	Sequence alignment	2,004

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17077488	Submitted genomic		NC_000012.12:g.120 852816_120852817in s115	GRCh38 (hg38)		NC_000012.12	Chr12	120,852,816	120,852,816
nssv17077488	Remapped	Perfect	NC_000012.11:g.121 290619_121290620in s115	GRCh37.p13	First Pass	NC_000012.11	Chr12	121,290,619	121,290,619

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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