A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698238



Internal ID15088204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15674526..15680635hg38UCSC Ensembl
Innerchr5:15674635..15680744hg19UCSC Ensembl
Innerchr5:15727635..15733744hg18UCSC Ensembl
Innerchr5:15727635..15733744hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386110
hg196110
hg186110
hg176110
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
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)nssv698238
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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