A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1699n100



Internal ID22787786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66520182..66591941hg38UCSC Ensembl
chr13:67094314..67166073hg19UCSC Ensembl
chr13:65992315..66064074hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3871760
hg1971760
hg1871760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048293, nsv1044410
Samples
Known GenesPCDH9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1699n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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