A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14315949



Internal ID22226236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:134668826..134668904hg38UCSC Ensembl
chr4:135589981..135590059hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3526151
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14315949
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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