A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2363n100



Internal ID19012731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20988537..22095238hg38UCSC Ensembl
chr15:21193866..22383189hg19UCSC Ensembl
chr15:19458525..19884553hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381106702
hg191189324
hg18426029
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054890, nsv1041550, nsv1042735, nsv1041497, nsv1044987, nsv1045714, nsv1039745, nsv1040922, nsv1049159, nsv1048559
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N4, 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)dgv2363n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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