A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538852



Internal ID18490447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22385562..23199681hg38UCSC Ensembl
Innerchr15:22673387..23487534hg19UCSC Ensembl
Innerchr15:20224751..21038975hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38814120
hg19814148
hg18814225
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038405
Supporting Variants
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)nssv3538852
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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