A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003819



Internal ID18845884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165974140..165974429hg38UCSC Ensembl
Outerchr4:166895292..166895581hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38290
hg19290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151253
Supporting Variants
SamplesKWB1
Known GenesTLL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003819
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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