A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053365



Internal ID18795896
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 StatusM
Merged Variantsdgv2408n100
Supporting Variantsnssv3538854
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)nsv1053365
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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