A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv865n100



Internal ID22786952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55150155..55457310hg38UCSC Ensembl
chr10:56909915..57217070hg19UCSC Ensembl
chr10:56579921..56887076hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38307156
hg19307156
hg18307156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043034, nsv1038046, nsv1045163
Samples
Known GenesRNU6-59P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv865n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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