A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3640693



Internal ID18938974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:59016641..59075412hg38UCSC Ensembl
Innerchr5:58312468..58371239hg19UCSC Ensembl
Innerchr5:58348225..58406996hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3858772
hg1958772
hg1858772
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032308
Supporting Variants
Samples
Known GenesPDE4D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3640693
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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