A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106726



Internal ID20673766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94507301..94507800hg38UCSC Ensembl
chr3:94226145..94226644hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362326
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.07267


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