A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv861n100



Internal ID20152477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:53792127..53821891hg38UCSC Ensembl
chr10:55551887..55581651hg19UCSC Ensembl
chr10:55221893..55251657hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3829765
hg1929765
hg1829765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051273, nsv1042430, nsv1052057
Samples
Known GenesPCDH15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv861n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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