A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2405n100



Internal ID22788492
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040788, nsv1037983, nsv1040720, nsv1046413, nsv1038863
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)dgv2405n100
Frequency
Sample Size11257
Observed Gain16
Observed Loss21
Observed Complex0
Frequencyn/a


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