A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538864



Internal ID18837145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22572335..23121986hg38UCSC Ensembl
Innerchr15:22751082..23300761hg19UCSC Ensembl
Innerchr15:20302446..20852202hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38549652
hg19549680
hg18549757
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1046413
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, LOC283683, 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)nssv3538864
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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