A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516558



Internal ID15443851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56547821..56580160hg38UCSC Ensembl
Innerchr11:56315297..56347636hg19UCSC Ensembl
Innerchr11:56071873..56104212hg18UCSC Ensembl
Innerchr11:56071873..56104212hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3832340
hg1932340
hg1832340
hg1732340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv669146, nssv681187, nssv673021, nssv656350, nssv686831, nssv685866, nssv659706, nssv659769, nssv692325, nssv661669
Samples
Known GenesOR5M10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516558
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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