A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703537



Internal ID15093503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:15717160..15719997hg38UCSC Ensembl
Innerchr5:15717269..15720106hg19UCSC Ensembl
Innerchr5:15770269..15773106hg18UCSC Ensembl
Innerchr5:15770269..15773106hg17UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382838
hg192838
hg182838
hg172838
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)nssv703537
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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