A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4766n54



Internal ID20138190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98648030..98650363hg38UCSC Ensembl
chr15:99191259..99193592hg19UCSC Ensembl
chr15:97008782..97011115hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382334
hg192334
hg182334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570707, nsv570706, nsv570708, nsv570704
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4766n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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