A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564506



Internal ID21888861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150268998..150269114hg38UCSC Ensembl
chr6:150590134..150590250hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019204
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564506
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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