A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11352n54



Internal ID22779247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54197894..54344915hg38UCSC Ensembl
chr7:54265587..54412608hg19UCSC Ensembl
chr7:54233081..54380102hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38147022
hg19147022
hg18147022
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607026, nsv607025, nsv607027
SamplesHGDP00210, HGDP00066, HGDP00157
Known GenesHPVC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11352n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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