A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv993n54



Internal ID22768888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:20543483..20576228hg38UCSC Ensembl
chr10:20832412..20865157hg19UCSC Ensembl
chr10:20872418..20905163hg18UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3832746
hg1932746
hg1832746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv550164, nsv550163, nsv550161
SamplesHGDP01187, HGDP01103, HGDP00779
Known GenesMIR4675
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv993n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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