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dbVar

Database of genomic structural variation

nsv5961016

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: 116 SVs from 24 studies. See in: genome view

Submitted genomic52,278,191-52,278,191

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5961016	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	52,278,191	52,278,191
nsv5961016	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	52,743,863	52,743,863

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17379689	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17379689	Submitted genomic		NC_000001.11:g.522 78191_52278192ins2 78	GRCh38 (hg38)		NC_000001.11	Chr1	52,278,191	52,278,191
nssv17379689	Remapped	Perfect	NC_000001.10:g.527 43863_52743864ins2 78	GRCh37.p13	First Pass	NC_000001.10	Chr1	52,743,863	52,743,863

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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