A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143540



Internal ID18915413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:55598024..55664124hg38UCSC Ensembl
Outerchr11:55365500..55431600hg19UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3866101
hg1966101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980747
SamplesKWS1
Known GenesOR4C11, OR4P4, OR4S2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143540
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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