A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2406n100



Internal ID22788493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22572335..23199681hg38UCSC Ensembl
chr15:22673387..23300761hg19UCSC Ensembl
chr15:20224751..20852202hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38627347
hg19627375
hg18627452
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040410, nsv1040861, nsv1037009, nsv1043900, nsv1040929, nsv1049600, nsv1053376, nsv1050103, nsv1042997, nsv1050356, nsv1046003, nsv1050262
Samples
Known GenesCYFIP1, GOLGA6L1, GOLGA8DP, GOLGA8I, HERC2P2, LOC283683, 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)dgv2406n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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