A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17563216



Internal ID21887571
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 StatusS
Merged Variantsnsv6015999
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17563216
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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