A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14314358



Internal ID22280937
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3196501
Supporting Variants
SamplesNA19239
Known GenesCXCL13
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14314358
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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