A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14318959



Internal ID22317625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152111644..152111747hg38UCSC Ensembl
chr4:153032796..153032899hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3207996
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14318959
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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