A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034656



Internal ID19123877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:59378898..59459754hg38UCSC Ensembl
Innerchr5:58674724..58755580hg19UCSC Ensembl
Innerchr5:58710481..58791337hg18UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg3880857
hg1980857
hg1880857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5683n100
Supporting Variantsnssv3747207
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)nsv1034656
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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