A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1700n100



Internal ID22787787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66691891..66770368hg38UCSC Ensembl
chr13:67266023..67344500hg19UCSC Ensembl
chr13:66164024..66242501hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3878478
hg1978478
hg1878478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050904, nsv1037808
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)dgv1700n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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