A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136141



Internal ID18913534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:118607285..118607885hg38UCSC Ensembl
Outerchr11:118478000..118478600hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989746
SamplesKWS2
Known GenesPHLDB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136141
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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