A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007251



Internal ID22068882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93964890..93968426hg38UCSC Ensembl
Outerchr11:93964792..93971294hg38UCSC Ensembl
Innerchr11:93698056..93701592hg19UCSC Ensembl
Outerchr11:93697958..93704460hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg386503
hg196503
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154761
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007251
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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