A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055096



Internal ID18797627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22483995..23199681hg38UCSC Ensembl
Innerchr15:22673387..23389101hg19UCSC Ensembl
Innerchr15:20224751..20940542hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38715687
hg19715715
hg18715792
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2407n100
Supporting Variantsnssv3715526, nssv3538839, nssv3538838
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8I, HERC2P2, 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)nsv1055096
Frequency
Sample Size29084
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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