A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219779



Internal ID22364692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:80482344..80482797hg38UCSC Ensembl
chr10:82242100..82242553hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354692
SamplesNA19238
Known GenesTSPAN14
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219779
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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