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dbVar

Database of genomic structural variation

nsv5974742

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: 163 SVs from 27 studies. See in: genome view

Submitted genomic59,569,700-59,569,700

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5974742	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	59,569,700	59,569,700
nsv5974742	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	57,647,061	57,647,061

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17380679	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17380679	Submitted genomic		NC_000017.11:g.595 69700_59569701ins1 80	GRCh38 (hg38)		NC_000017.11	Chr17	59,569,700	59,569,700
nssv17380679	Remapped	Perfect	NC_000017.10:g.576 47061_57647062ins1 80	GRCh37.p13	First Pass	NC_000017.10	Chr17	57,647,061	57,647,061

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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