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dbVar

Database of genomic structural variation

nsv5953190

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: 268 SVs from 38 studies. See in: genome view

Submitted genomic154,268,951-154,268,951

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5953190	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	154,268,951	154,268,951
nsv5953190	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	153,966,036	153,966,036

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17433216	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17433216	Submitted genomic		NC_000007.14:g.154 268951_154268952in s312	GRCh38 (hg38)		NC_000007.14	Chr7	154,268,951	154,268,951
nssv17433216	Remapped	Perfect	NC_000007.13:g.153 966036_153966037in s312	GRCh37.p13	First Pass	NC_000007.13	Chr7	153,966,036	153,966,036

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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