A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538854



Internal ID18490449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:22358243..23199681hg38UCSC Ensembl
Innerchr15:22673387..23645352hg19UCSC Ensembl
Innerchr15:20224751..21196793hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38841439
hg19971966
hg18972043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053365
Supporting Variants
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8EP, GOLGA8I, GOLGA8S, HERC2P2, HERC2P7, LOC283683, LOC440243, 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)nssv3538854
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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