A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517321



Internal ID15444614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:120787749..120797214hg38UCSC Ensembl
Innerchr9:123550027..123559492hg19UCSC Ensembl
Innerchr9:122589848..122599313hg18UCSC Ensembl
Innerchr9:120629581..120639046hg17UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg389466
hg199466
hg189466
hg179466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv685989, nssv651713, nssv677381, nssv681052, nssv667764, nssv682531
Samples
Known GenesFBXW2, LOC100288842
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517321
Frequency
Sample Size2026
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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