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dbVar

Database of genomic structural variation

nsv5950150

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: 149 SVs from 36 studies. See in: genome view

Submitted genomic78,249,064-78,249,064

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5950150	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	78,249,064	78,249,064
nsv5950150	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	79,170,218	79,170,218

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17415007	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17415007	Submitted genomic		NC_000004.12:g.782 49064_78249065ins5 6	GRCh38 (hg38)		NC_000004.12	Chr4	78,249,064	78,249,064
nssv17415007	Remapped	Perfect	NC_000004.11:g.791 70218_79170219ins5 6	GRCh37.p13	First Pass	NC_000004.11	Chr4	79,170,218	79,170,218

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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