A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3584561



Internal ID18770031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2037203..2259318hg38UCSC Ensembl
Innerchr8:1985345..2205102hg19UCSC Ensembl
Innerchr8:1972752..2192509hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38222116
hg19219758
hg18219758
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv65e213
Supporting Variantsessv9837830
SamplesKSF005
Known GenesMIR7160, MYOM2
MethodSNP array
AnalysisWe applied stringent filtering criteria such that CNV had to be a minimum of 1 kb and span 5 consecutive probes, and be detected by at least 2 out of the 3 algorithms. In addition we excluded CNVs that were on the X and Y-chromosomes, or approximately 300 kb adjacent to the centromeres and telomeres.
PlatformAffymetrix Genome-Wide Human SNP Array 6.0
Comments
ReferenceMokhtar_et_al_2014
Pubmed ID24956385
Accession Number(s)esv3584561
Frequency
Sample Size34
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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