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dbVar

Database of genomic structural variation

nsv5615367

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: 143 SVs from 38 studies. See in: genome view

Submitted genomic113,603,789-113,603,789

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5615367	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	113,603,789	113,603,789
nsv5615367	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	114,361,366	114,361,366

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17107880	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
nssv17107880	Submitted genomic		NC_000002.12:g.113 603789_113603790in s160	GRCh38 (hg38)		NC_000002.12	Chr2	113,603,789	113,603,789
nssv17107880	Remapped	Perfect	NC_000002.11:g.114 361366_114361367in s160	GRCh37.p13	First Pass	NC_000002.11	Chr2	114,361,366	114,361,366

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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