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dbVar

Database of genomic structural variation

nsv5961748

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: 96 SVs from 25 studies. See in: genome view

Submitted genomic129,763,210-129,763,210

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961748	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000003.12	Chr3	129,763,210	129,763,210
nsv5961748	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000003.11	Chr3	129,482,053	129,482,053

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17408229	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17408229	Submitted genomic		NC_000003.12:g.129 763210_129763211in s240	GRCh38 (hg38)		NC_000003.12	Chr3	129,763,210	129,763,210
nssv17408229	Remapped	Perfect	NC_000003.11:g.129 482053_129482054in s240	GRCh37.p13	First Pass	NC_000003.11	Chr3	129,482,053	129,482,053

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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