A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14317052



Internal ID22190881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:158471977..158476179hg38UCSC Ensembl
chr4:159393129..159397331hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg384203
hg194203
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3206265
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14317052
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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