A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522706



Internal ID8416981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120303136..120307923hg38UCSC Ensembl
Innerchr11:120173845..120178632hg19UCSC Ensembl
Innerchr11:119679055..119683842hg18UCSC Ensembl
Innerchr11:119679055..119683842hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg384788
hg194788
hg184788
hg174788
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv706118
Samples
Known GenesPOU2F3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522706
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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