A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521908



Internal ID15102515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168162543..168167754hg38UCSC Ensembl
Innerchr4:169083694..169088905hg19UCSC Ensembl
Innerchr4:169320269..169325480hg18UCSC Ensembl
Innerchr4:169458424..169463635hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg385212
hg195212
hg185212
hg175212
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694679
Samples
Known GenesANXA10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521908
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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