A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2583n100



Internal ID20154199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43553212..43698816hg38UCSC Ensembl
chr15:43845410..43991014hg19UCSC Ensembl
chr15:41632702..41778306hg18UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38145605
hg19145605
hg18145605
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039818, nsv1048041
Samples
Known GenesCATSPER2, CKMT1A, CKMT1B, PPIP5K1, RNU6-28P, STRC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2583n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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