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dbVar

Database of genomic structural variation

nsv5968958

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: 144 SVs from 22 studies. See in: genome view

Submitted genomic66,406,585-66,406,585

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5968958	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	66,406,585	66,406,585
nsv5968958	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	64,402,703	64,402,703

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17371263	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17371263	Submitted genomic		NC_000017.11:g.664 06585_66406586ins2 42	GRCh38 (hg38)		NC_000017.11	Chr17	66,406,585	66,406,585
nssv17371263	Remapped	Perfect	NC_000017.10:g.644 02703_64402704ins2 42	GRCh37.p13	First Pass	NC_000017.10	Chr17	64,402,703	64,402,703

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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