A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14321694



Internal ID22275756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:114241708..114241794hg38UCSC Ensembl
chr5:113577405..113577491hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209476
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14321694
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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