A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316810



Internal ID22130251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:184234142..184234612hg38UCSC Ensembl
chr4:185155295..185155765hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190803
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316810
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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