A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv596965



Internal ID16384374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6713146..6719051hg38UCSC Ensembl
Innerchr5:6713259..6719164hg19UCSC Ensembl
Innerchr5:6766259..6772164hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385906
hg195906
hg185906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1023762
Samples
Known GenesPAPD7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv596965
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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