A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379368



Internal ID22233768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:49142084..49147725hg38UCSC Ensembl
chr15:49434281..49439922hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385642
hg195642
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212243
Supporting Variants
SamplesHG00733
Known GenesCOPS2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379368
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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