A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006360



Internal ID21915703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33832623..33832783hg38UCSC Ensembl
chr6:33800400..33800560hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006360
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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