A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5786n100



Internal ID22791873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114600122..114685855hg38UCSC Ensembl
chr5:113935819..114021552hg19UCSC Ensembl
chr5:113963718..114049451hg18UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3885734
hg1985734
hg1885734
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1019344, nsv1021807
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv5786n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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