A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3218078



Internal ID22363543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77428962..77429250hg38UCSC Ensembl
chr15:77721304..77721592hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14375740
SamplesNA19240
Known GenesHMG20A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3218078
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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