A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525787



Internal ID15453080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:87178242..87209136hg38UCSC Ensembl
Innerchr11:86889284..86920178hg19UCSC Ensembl
Innerchr11:86566932..86597826hg18UCSC Ensembl
Innerchr11:86566932..86597826hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3830895
hg1930895
hg1830895
hg1730895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701965
Samples
Known GenesTMEM135
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525787
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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