A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2534n100



Internal ID19012902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31059860..31100684hg38UCSC Ensembl
chr15:31352063..31392887hg19UCSC Ensembl
chr15:29139355..29180179hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3840825
hg1940825
hg1840825
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046535, nsv1037745, nsv1048746, nsv1037693
Samples
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2534n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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