A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv998n100



Internal ID20152614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132998894..133170978hg38UCSC Ensembl
chr10:134812398..134984482hg19UCSC Ensembl
chr10:134662388..134834472hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38172085
hg19172085
hg18172085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044664, nsv1043942
Samples
Known GenesGPR123, KNDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv998n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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