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dbVar

Database of genomic structural variation

nsv5655782

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: 110 SVs from 32 studies. See in: genome view

Submitted genomic120,561,098-120,561,098

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5655782	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000012.12	Chr12	120,561,098	120,561,098
nsv5655782	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000012.11	Chr12	120,998,901	120,998,901

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17077477	insertion	SAMN00000485	Sequencing	Sequence alignment	1,404

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17077477	Submitted genomic		NC_000012.12:g.120 561098_120561099in s348	GRCh38 (hg38)		NC_000012.12	Chr12	120,561,098	120,561,098
nssv17077477	Remapped	Perfect	NC_000012.11:g.120 998901_120998902in s348	GRCh37.p13	First Pass	NC_000012.11	Chr12	120,998,901	120,998,901

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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