A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17572185



Internal ID21764228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:132692640..132692703hg38UCSC Ensembl
chr6:133013779..133013842hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016760
Supporting Variants
Samples
Known GenesVNN1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17572185
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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