A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14375982



Internal ID22125740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62332153..62332596hg38UCSC Ensembl
chr15:62624352..62624795hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3528804
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14375982
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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