A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1033361



Internal ID15886547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:60190941..60197935hg38UCSC Ensembl
Innerchr5:59486768..59493762hg19UCSC Ensembl
Innerchr5:59522525..59529519hg18UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg386995
hg196995
hg186995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv598261
Supporting Variants
Samples
Known GenesPDE4D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1033361
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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