A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017859



Internal ID21927202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:6228528..6355787hg38UCSC Ensembl
chr8:6086049..6213308hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38127260
hg19127260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017859
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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