A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113448



Internal ID18917407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:131680369..131680451hg38UCSC Ensembl
Outerchr11:131550263..131550345hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968738
SamplesKWS2
Known GenesNTM
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113448
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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