A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016600



Internal ID21925943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167575681..167575745hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3865
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576963
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016600
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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