A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv362n21



Internal ID20132083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:176878677..176889200hg38UCSC Ensembl
chr5:176305678..176316201hg19UCSC Ensembl
chr5:176238284..176248807hg18UCSC Ensembl
chr5:176238284..176248807hg17UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg3810524
hg1910524
hg1810524
hg1710524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv526781, nsv517492
Samples
Known GenesHK3, UNC5A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv362n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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