A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9751n54



Internal ID22777646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:45854525..46287010hg38UCSC Ensembl
chr5:45854627..46287112hg19UCSC Ensembl
chr5:45890384..46322869hg18UCSC Ensembl
Cytoband5p11
Allele length
AssemblyAllele length
hg38432486
hg19432486
hg18432486
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597999, nsv598001, nsv598000
Samples1780854532_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9751n54
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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