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dbVar

Database of genomic structural variation

nsv5961369

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: 129 SVs from 29 studies. See in: genome view

Submitted genomic141,407,491-141,407,491

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961369	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	141,407,491	141,407,491
nsv5961369	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	140,787,058	140,787,058

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423459	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423459	Submitted genomic		NC_000005.10:g.141 407491_141407492in s400	GRCh38 (hg38)		NC_000005.10	Chr5	141,407,491	141,407,491
nssv17423459	Remapped	Perfect	NC_000005.9:g.1407 87058_140787059ins 400	GRCh37.p13	First Pass	NC_000005.9	Chr5	140,787,058	140,787,058

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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