A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531209



Internal ID18829490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76651624..76740752hg38UCSC Ensembl
Innerchr14:77117967..77207095hg19UCSC Ensembl
Innerchr14:76187720..76276848hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3889129
hg1989129
hg1889129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045997
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531209
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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