A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011839



Internal ID21921182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102293688..102293816hg38UCSC Ensembl
chr6:102741563..102741691hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566856
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011839
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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