A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv975n100



Internal ID20152591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110964401..111035401hg38UCSC Ensembl
chr10:112724159..112795159hg19UCSC Ensembl
chr10:112714149..112785149hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3871001
hg1971001
hg1871001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051595, nsv1048444, nsv1036202
Samples
Known GenesSHOC2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv975n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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