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dbVar

Database of genomic structural variation

nsv5966073

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: 94 SVs from 26 studies. See in: genome view

Submitted genomic38,990,692-38,990,692

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5966073	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	38,990,692	38,990,692
nsv5966073	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	38,990,794	38,990,794

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17417581	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17417581	Submitted genomic		NC_000005.10:g.389 90692_38990693ins6 7	GRCh38 (hg38)		NC_000005.10	Chr5	38,990,692	38,990,692
nssv17417581	Remapped	Perfect	NC_000005.9:g.3899 0794_38990795ins67	GRCh37.p13	First Pass	NC_000005.9	Chr5	38,990,794	38,990,794

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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