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dbVar

Database of genomic structural variation

nsv5605472

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: 97 SVs from 21 studies. See in: genome view

Submitted genomic69,684,528-69,684,528

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5605472	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	69,684,528	69,684,528
nsv5605472	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	69,911,660	69,911,660

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17113603	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
nssv17113603	Submitted genomic		NC_000002.12:g.696 84528_69684529ins3 59	GRCh38 (hg38)		NC_000002.12	Chr2	69,684,528	69,684,528
nssv17113603	Remapped	Perfect	NC_000002.11:g.699 11660_69911661ins3 59	GRCh37.p13	First Pass	NC_000002.11	Chr2	69,911,660	69,911,660

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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