A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3223556



Internal ID22367288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80900104..80900677hg38UCSC Ensembl
chr15:81192445..81193018hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14373768
SamplesNA19239
Known GenesKIAA1199
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3223556
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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