A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517409



Internal ID15098016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:98436902..98463263hg38UCSC Ensembl
Innerchr13:99089156..99115517hg19UCSC Ensembl
Innerchr13:97887157..97913518hg18UCSC Ensembl
Innerchr13:97887157..97913518hg17UCSC Ensembl
Cytoband13q32.2
Allele length
AssemblyAllele length
hg3826362
hg1926362
hg1826362
hg1726362
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694284, nssv688464, nssv679894, nssv675599, nssv655062, nssv701177, nssv689645, nssv659415, nssv651934, nssv668306, nssv696029
Samples
Known GenesFARP1, STK24
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517409
Frequency
Sample Size2026
Observed Gain1
Observed Loss10
Observed Complex0
Frequencyn/a


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