A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv569993



Internal ID16010716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:74949814..75191411hg38UCSC Ensembl
Innerchr15:75242155..75483752hg19UCSC Ensembl
Innerchr15:73029208..73270805hg18UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38241598
hg19241598
hg18241598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv845287
Samples
Known GenesPPCDC, RPP25, SCAMP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv569993
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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