A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523894



Internal ID15451187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:6315326..6325419hg38UCSC Ensembl
Innerchr5:6315439..6325532hg19UCSC Ensembl
Innerchr5:6368439..6378532hg18UCSC Ensembl
Innerchr5:6368439..6378532hg17UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3810094
hg1910094
hg1810094
hg1710094
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699737
Samples
Known GenesFLJ33360
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523894
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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