A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560392



Internal ID21884747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132600758..132601170hg38UCSC Ensembl
chr6:132921897..132922309hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004057
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560392
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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