A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524537



Internal ID15105144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:77872220..77882175hg38UCSC Ensembl
Innerchr11:77583266..77593221hg19UCSC Ensembl
Innerchr11:77260914..77270869hg18UCSC Ensembl
Innerchr11:77260914..77270869hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg389956
hg199956
hg189956
hg179956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700487
Samples
Known GenesAAMDC, INTS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524537
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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