A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659706



Internal ID15396358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56557100..56580160hg38UCSC Ensembl
Innerchr11:56324576..56347636hg19UCSC Ensembl
Innerchr11:56081152..56104212hg18UCSC Ensembl
Innerchr11:56081152..56104212hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3823061
hg1923061
hg1823061
hg1723061
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516558
Supporting Variants
Samples
Known GenesOR5M10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659706
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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