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dbVar

Database of genomic structural variation

nsv5619107

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: 659 SVs from 41 studies. See in: genome view

Submitted genomic2,522,791-2,522,791

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5619107	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	2,522,791	2,522,791
nsv5619107	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	2,454,230	2,454,230

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17064631	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17064631	Submitted genomic		NC_000001.11:g.252 2791_2522792ins556	GRCh38 (hg38)		NC_000001.11	Chr1	2,522,791	2,522,791
nssv17064631	Remapped	Perfect	NC_000001.10:g.245 4230_2454231ins556	GRCh37.p13	First Pass	NC_000001.10	Chr1	2,454,230	2,454,230

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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