A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv696n100



Internal ID22786783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27318256..27424596hg38UCSC Ensembl
chr10:27607185..27713525hg19UCSC Ensembl
chr10:27647191..27753531hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38106341
hg19106341
hg18106341
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043338, nsv1054468, nsv1049369, nsv1045904, nsv1052878, nsv1053549, nsv1038408, nsv1053324, nsv1044075, nsv1042004, nsv1054401, nsv1042483, nsv1049772
Samples
Known GenesPTCHD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv696n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss76
Observed Complex0
Frequencyn/a


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