A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv336n21



Internal ID22766528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:18676765..18738188hg38UCSC Ensembl
chr5:18676874..18738297hg19UCSC Ensembl
chr5:18712631..18774054hg18UCSC Ensembl
chr5:18712631..18774054hg17UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg3861424
hg1961424
hg1861424
hg1761424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv523077, nsv524117
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv336n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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