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dbVar

Database of genomic structural variation

nsv5955066

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: 156 SVs from 36 studies. See in: genome view

Submitted genomic155,147,380-155,147,380

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5955066	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000001.11	Chr1	155,147,380	155,147,380
nsv5955066	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000001.10	Chr1	155,119,856	155,119,856

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17362313	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17362313	Submitted genomic		NC_000001.11:g.155 147380_155147381in s85	GRCh38 (hg38)		NC_000001.11	Chr1	155,147,380	155,147,380
nssv17362313	Remapped	Perfect	NC_000001.10:g.155 119856_155119857in s85	GRCh37.p13	First Pass	NC_000001.10	Chr1	155,119,856	155,119,856

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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