A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135182



Internal ID18912238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:166083172..166083769hg38UCSC Ensembl
Outerchr4:167004324..167004921hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2935n106
Supporting Variantsnssv3988736
SamplesKWS2
Known GenesTLL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135182
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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