A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13679437



Internal ID21201295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121993748..121993924hg38UCSC Ensembl
chr12:122431654..122431830hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791830
Supporting Variants
Samples
Known GenesWDR66
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13679437
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.477273


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