A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531144



Internal ID18482739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:73248673..73273941hg38UCSC Ensembl
Innerchr14:73715381..73740649hg19UCSC Ensembl
Innerchr14:72785134..72810402hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3825269
hg1925269
hg1825269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1035179
Supporting Variants
Samples
Known GenesPAPLN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3531144
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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