A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528323



Internal ID22397710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81334368..81334467hg38UCSC Ensembl
chr8:82246603..82246702hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14341172, nssv14341171, nssv14341170, nssv14341169
SamplesNA19239, NA19240, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528323
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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