A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3216311



Internal ID22362342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83875281..83882622hg38UCSC Ensembl
chr10:85635037..85642378hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg387342
hg197342
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1001n152
Supporting Variantsnssv14354803, nssv14354804
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3216311
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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