A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518168



Internal ID15445461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:33465184..33478436hg38UCSC Ensembl
Innerchr9:33465182..33478434hg19UCSC Ensembl
Innerchr9:33455182..33468434hg18UCSC Ensembl
Innerchr9:33455182..33468434hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3813253
hg1913253
hg1813253
hg1713253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695589
Samples
Known GenesMIR6851, NOL6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518168
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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