A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531122



Internal ID18482717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70487432..70546518hg38UCSC Ensembl
Innerchr14:70954149..71013235hg19UCSC Ensembl
Innerchr14:70023902..70082988hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3859087
hg1959087
hg1859087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050615
Supporting Variants
Samples
Known GenesADAM20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531122
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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