A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9620n54



Internal ID22777515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16179085..16180058hg38UCSC Ensembl
chr5:16179194..16180167hg19UCSC Ensembl
chr5:16232194..16233167hg18UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597305, nsv597301, nsv597306, nsv597300
Samples
Known GenesMARCH11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9620n54
Frequency
Sample Size17421
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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