A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524611



Internal ID15451904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17279297..17294482hg38UCSC Ensembl
Innerchr11:17300844..17316029hg19UCSC Ensembl
Innerchr11:17257420..17272605hg18UCSC Ensembl
Innerchr11:17257420..17272605hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815186
hg1915186
hg1815186
hg1715186
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700572
Samples
Known GenesNUCB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524611
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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