A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005094



Internal ID21914437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:110562359..110562808hg38UCSC Ensembl
chr6:110883562..110884011hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38450
hg19450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005094
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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