A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14316183



Internal ID22141179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:103418242..103426708hg38UCSC Ensembl
chr4:104339399..104347865hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg388467
hg198467
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3209547
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14316183
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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