A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14307998



Internal ID22141759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34093225..34098991hg38UCSC Ensembl
chr3:34134717..34140483hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg385767
hg195767
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3202917
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14307998
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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