A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7692n100



Internal ID20159308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102880999..103104175hg38UCSC Ensembl
chr9:105643281..105866457hg19UCSC Ensembl
chr9:104683102..104906278hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38223177
hg19223177
hg18223177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047506, nsv1051059
Samples
Known GenesCYLC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7692n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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