A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527902



Internal ID15455195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:126149067..126158191hg38UCSC Ensembl
Innerchr9:128911346..128920470hg19UCSC Ensembl
Innerchr9:127951167..127960291hg18UCSC Ensembl
Innerchr9:125990900..126000024hg17UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg389125
hg199125
hg189125
hg179125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704406
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527902
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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