A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694879



Internal ID15084845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:38503356..38529801hg38UCSC Ensembl
Innerchr5:38503458..38529903hg19UCSC Ensembl
Innerchr5:38539215..38565660hg18UCSC Ensembl
Innerchr5:38539215..38565660hg17UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3826446
hg1926446
hg1826446
hg1726446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516065
Supporting Variants
Samples
Known GenesLIFR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694879
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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