A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13681253



Internal ID21203113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44034107..44034281hg38UCSC Ensembl
chr3:44075599..44075773hg19UCSC Ensembl
Cytoband3p21.33
Allele length
AssemblyAllele length
hg38175
hg19175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2809452
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13681253
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.296875


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