A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1254n54



Internal ID22769149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69523734..69537212hg38UCSC Ensembl
chr10:71283490..71296968hg19UCSC Ensembl
chr10:70953496..70966974hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3813479
hg1913479
hg1813479
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv551459, nsv551471
SamplesHGDP00717, HGDP00750, HGDP01312, HGDP00956, HGDP01333, HGDP01331, HGDP01038
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv1254n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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