A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14382627



Internal ID22195704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691161..68691624hg38UCSC Ensembl
chr15:68983500..68983963hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3212041
Supporting Variants
SamplesHG00731
Known GenesCORO2B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14382627
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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