A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527214



Internal ID15454507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88127478..88140064hg38UCSC Ensembl
Innerchr11:87860646..87873232hg19UCSC Ensembl
Innerchr11:87500294..87512880hg18UCSC Ensembl
Innerchr11:87500294..87512880hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3812587
hg1912587
hg1812587
hg1712587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703614
Samples
Known GenesRAB38
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527214
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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