A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656238



Internal ID15046204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15113954..15870191hg38UCSC Ensembl
Innerchr5:15114063..15870300hg19UCSC Ensembl
Innerchr5:15167063..15923300hg18UCSC Ensembl
Innerchr5:15167063..15923300hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38756238
hg19756238
hg18756238
hg17756238
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)nssv656238
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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