A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14323655



Internal ID22287225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149111962..149111962hg38UCSC Ensembl
chr5:148491525..148491525hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3564141
Supporting Variants
SamplesNA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14323655
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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