A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015001



Internal ID21924344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138128699..138128808hg38UCSC Ensembl
chr6:138449836..138449945hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576652
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015001
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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