A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1323n54



Internal ID18993499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86655778..86658344hg38UCSC Ensembl
chr10:88415535..88418101hg19UCSC Ensembl
chr10:88405515..88408081hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382567
hg192567
hg182567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551790, nsv551792, nsv551791
Samples
Known GenesOPN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1323n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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