A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015999



Internal ID21925342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102430372..102555660hg38UCSC Ensembl
chr6:102878247..103003535hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38125289
hg19125289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015999
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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