Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5952012

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: 141 SVs from 30 studies. See in: genome view

Submitted genomic78,483,769-78,483,769

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5952012	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	78,483,769	78,483,769
nsv5952012	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	79,404,923	79,404,923

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17418327	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17418327	Submitted genomic		NC_000004.12:g.784 83769_78483770ins1 85	GRCh38 (hg38)		NC_000004.12	Chr4	78,483,769	78,483,769
nssv17418327	Remapped	Perfect	NC_000004.11:g.794 04923_79404924ins1 85	GRCh37.p13	First Pass	NC_000004.11	Chr4	79,404,923	79,404,923

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.

You are here: NCBI