A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219653



Internal ID22364607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25966890..25966998hg38UCSC Ensembl
chr15:26212037..26212145hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2855n152
Supporting Variantsnssv14377457, nssv14376228, nssv14376848, nssv14388473
SamplesNA19238, HG00731, NA19240, HG00513
Known GenesLOC100128714
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219653
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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