A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4627n54



Internal ID22772522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75201482..75248150hg38UCSC Ensembl
chr15:75493823..75540491hg19UCSC Ensembl
chr15:73280876..73327544hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3846669
hg1946669
hg1846669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569996, nsv569995
Samples
Known GenesC15orf39
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4627n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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