A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529023



Internal ID15109630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38955694..39119621hg38UCSC Ensembl
Innerchr5:38955796..39119723hg19UCSC Ensembl
Innerchr5:38991553..39155480hg18UCSC Ensembl
Innerchr5:38991553..39155480hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38163928
hg19163928
hg18163928
hg17163928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705734
Samples
Known GenesFYB, RICTOR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529023
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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