A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538870



Internal ID18490465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22385562..23121986hg38UCSC Ensembl
Innerchr15:22751082..23487534hg19UCSC Ensembl
Innerchr15:20302446..21038975hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38736425
hg19736453
hg18736530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042107
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA8EP, GOLGA8I, HERC2P2, HERC2P7, 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)nssv3538870
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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