A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660846



Internal ID15050812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15659949..15723524hg38UCSC Ensembl
Innerchr5:15660058..15723633hg19UCSC Ensembl
Innerchr5:15713058..15776633hg18UCSC Ensembl
Innerchr5:15713058..15776633hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3863576
hg1963576
hg1863576
hg1763576
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516929
Supporting Variants
Samples
Known GenesFBXL7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660846
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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