A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9732n54



Internal ID20143156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42628506..42630189hg38UCSC Ensembl
chr5:42628608..42630291hg19UCSC Ensembl
chr5:42664365..42666048hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg381684
hg191684
hg181684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597889, nsv597890, nsv597891, nsv597888
Samples
Known GenesGHR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9732n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer