A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9736n54



Internal ID20143160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42629911..42630866hg38UCSC Ensembl
chr5:42630013..42630968hg19UCSC Ensembl
chr5:42665770..42666725hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38956
hg19956
hg18956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597912, nsv597923, nsv597920, nsv597918, nsv597914, nsv597915, nsv597913, nsv597919, nsv597922, nsv597910, nsv597924, nsv597917, nsv597911, nsv597921
Samples
Known GenesGHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9736n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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