A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6722n54



Internal ID22774617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18003906..18070689hg38UCSC Ensembl
chr2:18185172..18251955hg19UCSC Ensembl
chr2:18048653..18115436hg18UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3866784
hg1966784
hg1866784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv581108, nsv581109
SamplesHGDP00007
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv6722n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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