A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4428n54



Internal ID18996604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31064222..31102334hg38UCSC Ensembl
chr15:31356425..31394537hg19UCSC Ensembl
chr15:29143717..29181829hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3838113
hg1938113
hg1838113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv568769, nsv568771, nsv568768, nsv568770
Samples1780854419_A
Known GenesMIR211, TRPM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4428n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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