A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538812



Internal ID18490407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22764978..23199681hg38UCSC Ensembl
Innerchr15:22673387..23108132hg19UCSC Ensembl
Innerchr15:20224751..20659573hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38434704
hg19434746
hg18434823
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041725
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, LOC283683, MIR4509-1, MIR4509-2, MIR4509-3, NIPA1, NIPA2, TUBGCP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3538812
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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