A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569524



Internal ID16010247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55266426..55320313hg38UCSC Ensembl
Innerchr15:55558624..55612511hg19UCSC Ensembl
Innerchr15:53345916..53399803hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3853888
hg1953888
hg1853888
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv843334
Samples
Known GenesPIGB, RAB27A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569524
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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