A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4765n54



Internal ID22772660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98648030..98649896hg38UCSC Ensembl
chr15:99191259..99193125hg19UCSC Ensembl
chr15:97008782..97010648hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381867
hg191867
hg181867
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570703, nsv570702
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4765n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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