A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667764



Internal ID15404416
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517321
Supporting Variants
Samples
Known GenesFBXW2, LOC100288842
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667764
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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