A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1131841



Internal ID18903580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165953581..165953633hg38UCSC Ensembl
Outerchr4:166874733..166874785hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986415
SamplesKWS1
Known GenesTLL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1131841
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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