A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv974n100



Internal ID20152590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110924064..111035401hg38UCSC Ensembl
chr10:112683822..112795159hg19UCSC Ensembl
chr10:112673812..112785149hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38111338
hg19111338
hg18111338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048809, nsv1042020
Samples
Known GenesRPL13AP6, SHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv974n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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