A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113434



Internal ID19264112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:111358310..111358392hg38UCSC Ensembl
Outerchr11:111229035..111229117hg19UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971655, nssv3982901
SamplesKWS2, KWS1
Known GenesPOU2AF1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113434
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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