A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530701



Internal ID18828982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:19869145..19934411hg38UCSC Ensembl
Innerchr14:20337304..20402570hg19UCSC Ensembl
Innerchr14:19407144..19472410hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3865267
hg1965267
hg1865267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041442
Supporting Variants
Samples
Known GenesOR4K2, OR4K5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3530701
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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