A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584833



Internal ID18536428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:44870663..44920098hg38UCSC Ensembl
Innerchr20:43499304..43548739hg19UCSC Ensembl
Innerchr20:42932718..42982153hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3849436
hg1949436
hg1849436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062628
Supporting Variants
Samples
Known GenesPABPC1L, YWHAB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584833
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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