A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4317n54



Internal ID20137741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22770773..23122763hg38UCSC Ensembl
chr15:22750305..23102295hg19UCSC Ensembl
chr15:20301669..20653736hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38351991
hg19351991
hg18352068
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568229, nsv568247, nsv568246, nsv568231, nsv568230, nsv568222, nsv568223, nsv568241
Samples
Known GenesCYFIP1, LOC283683, NIPA1, NIPA2, TUBGCP5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4317n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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