A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570392



Internal ID16011115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90282201..90455896hg38UCSC Ensembl
Innerchr15:90825433..90999128hg19UCSC Ensembl
Innerchr15:88626437..88800132hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38173696
hg19173696
hg18173696
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4705n54
Supporting Variantsnssv1149605
Samples1798860114_A
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570392
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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