A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011542



Internal ID21920885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:108264298..108264353hg38UCSC Ensembl
chr6:108585502..108585557hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568975
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011542
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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