A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2408n100



Internal ID20154024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22358243..23199681hg38UCSC Ensembl
chr15:22673387..23645352hg19UCSC Ensembl
chr15:20224751..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 Variants
Supporting Variantsnsv1053365, nsv1037010, nsv1053792, nsv1038737
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)dgv2408n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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