A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9735n54



Internal ID20143159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42629911..42630636hg38UCSC Ensembl
chr5:42630013..42630738hg19UCSC Ensembl
chr5:42665770..42666495hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38726
hg19726
hg18726
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597909, nsv597916, nsv597908
Samples
Known GenesGHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9735n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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