A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3712277



Internal ID18663872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:35058033..35255021hg38UCSC Ensembl
Innerchr14:35527239..35724227hg19UCSC Ensembl
Innerchr14:34596990..34793978hg18UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg38196989
hg19196989
hg18196989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046992
Supporting Variants
Samples
Known GenesFAM177A1, KIAA0391, PPP2R3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3712277
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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