A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527285



Internal ID15107892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:106013358..106020872hg38UCSC Ensembl
Innerchr11:105884085..105891599hg19UCSC Ensembl
Innerchr11:105389295..105396809hg18UCSC Ensembl
Innerchr11:105389295..105396809hg17UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg387515
hg197515
hg187515
hg177515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv81n21
Supporting Variantsnssv703699
Samples
Known GenesMSANTD4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527285
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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