A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525637



Internal ID15452930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:56563070..56599201hg38UCSC Ensembl
Innerchr11:56330546..56366677hg19UCSC Ensembl
Innerchr11:56087122..56123253hg18UCSC Ensembl
Innerchr11:56087122..56123253hg17UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3836132
hg1936132
hg1836132
hg1736132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv69n21
Supporting Variantsnssv701791
Samples
Known GenesOR5M10
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525637
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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