A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528804



Internal ID22398196
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2953n152
Supporting Variantsnssv14391730, nssv14375982, nssv14373276, nssv14376791, nssv14386092, nssv14384970
SamplesHG00512, NA19238, NA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528804
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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