A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2245n100



Internal ID22788332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20327352..20913755hg38UCSC Ensembl
chr15:20532605..21119084hg19UCSC Ensembl
chr15:18792619..19383709hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38586404
hg19586480
hg18591091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050684, nsv1051191, nsv1054335, nsv1047565, nsv1037437, nsv1037572, nsv1037177, nsv1047579, nsv1045272, nsv1042923, nsv1037942, nsv1035467, nsv1036968, nsv1037604, nsv1041128, nsv1043174
Samples
Known GenesCXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2245n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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