A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528803



Internal ID15456096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98236372..98270562hg38UCSC Ensembl
Innerchr13:98888626..98922816hg19UCSC Ensembl
Innerchr13:97686627..97720817hg18UCSC Ensembl
Innerchr13:97686627..97720817hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3834191
hg1934191
hg1834191
hg1734191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705477
Samples
Known GenesFARP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528803
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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