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dbVar

Database of genomic structural variation

nsv5969787

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Almarri et al. 2020

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

Submitted genomic70,065,601-70,065,601

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5969787	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	70,065,601	70,065,601
nsv5969787	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	68,061,742	68,061,742

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17373148	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17373148	Submitted genomic		NC_000017.11:g.700 65601_70065602ins3 16	GRCh38 (hg38)		NC_000017.11	Chr17	70,065,601	70,065,601
nssv17373148	Remapped	Perfect	NC_000017.10:g.680 61742_68061743ins3 16	GRCh37.p13	First Pass	NC_000017.10	Chr17	68,061,742	68,061,742

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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