A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145559



Internal ID19284444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:88336370..88359026hg38UCSC Ensembl
Outerchr11:88069538..88092194hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3822657
hg1922657
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983201
SamplesKWS1
Known GenesCTSC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145559
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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