A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11493n54



Internal ID20144917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88519150..90265948hg38UCSC Ensembl
chr7:88148465..89895262hg19UCSC Ensembl
chr7:87986401..89733198hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381746799
hg191746798
hg181746798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607742, nsv607744, nsv607743, nsv607741
Samples1780854574_A
Known GenesC7orf62, C7orf63, DPY19L2P4, STEAP1, STEAP2, ZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11493n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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