A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6020267



Internal ID21929610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:81132781..81134383hg38UCSC Ensembl
chr8:82045016..82046618hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6020267
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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