A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11200n54



Internal ID22779095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:10123160..10180922hg38UCSC Ensembl
chr7:10162787..10220549hg19UCSC Ensembl
chr7:10129312..10187074hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3857763
hg1957763
hg1857763
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606186, nsv606184, nsv606185
SamplesHGDP01052, HGDP01041, HGDP01045
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11200n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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