A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038737



Internal ID18781268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22390747..23199681hg38UCSC Ensembl
Innerchr15:22673387..23482349hg19UCSC Ensembl
Innerchr15:20224751..21033790hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38808935
hg19808963
hg18809040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2408n100
Supporting Variantsnssv3538850
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8EP, GOLGA8I, HERC2P2, HERC2P7, LOC283683, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038737
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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