A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4800n54



Internal ID20138224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101663675..101752560hg38UCSC Ensembl
chr15:102203878..102292763hg19UCSC Ensembl
chr15:100021401..100110286hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3888886
hg1988886
hg1888886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570907, nsv570908, nsv570909
Samples
Known GenesTARSL2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4800n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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