A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3196501



Internal ID22346500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77562591..77562710hg38UCSC Ensembl
chr4:78483745..78483864hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14314358
SamplesNA19239
Known GenesCXCL13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3196501
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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