A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528117



Internal ID15455410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88453960..88465762hg38UCSC Ensembl
Innerchr11:88187128..88198930hg19UCSC Ensembl
Innerchr11:87826776..87838578hg18UCSC Ensembl
Innerchr11:87826776..87838578hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3811803
hg1911803
hg1811803
hg1711803
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv77n21
Supporting Variantsnssv704660
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528117
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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