A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522018



Internal ID15449311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:99606259..99624424hg38UCSC Ensembl
Innerchr9:102368541..102386706hg19UCSC Ensembl
Innerchr9:101408362..101426527hg18UCSC Ensembl
Innerchr9:99448096..99466261hg17UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3818166
hg1918166
hg1818166
hg1718166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694119
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522018
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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