A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4764n54



Internal ID22772659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98647653..98650539hg38UCSC Ensembl
chr15:99190882..99193768hg19UCSC Ensembl
chr15:97008405..97011291hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382887
hg192887
hg182887
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv570696, nsv570698
Samples
Known GenesIGF1R
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4764n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss2
Observed Complex0
Frequencyn/a


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