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dbVar

Database of genomic structural variation

nsv5950031

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: 165 SVs from 31 studies. See in: genome view

Submitted genomic140,362,274-140,362,274

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5950031	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000004.12	Chr4	140,362,274	140,362,274
nsv5950031	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000004.11	Chr4	141,283,428	141,283,428

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423502	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423502	Submitted genomic		NC_000004.12:g.140 362274_140362275in s66	GRCh38 (hg38)		NC_000004.12	Chr4	140,362,274	140,362,274
nssv17423502	Remapped	Perfect	NC_000004.11:g.141 283428_141283429in s66	GRCh37.p13	First Pass	NC_000004.11	Chr4	141,283,428	141,283,428

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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