A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560680



Internal ID21885035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:31980532..32046126hg38UCSC Ensembl
chr6:31948309..32013903hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3865595
hg1965595
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007166
Supporting Variants
Samples
Known GenesC4A, C4B, C4B_2, CYP21A1P, CYP21A2, STK19, TNXA, TNXB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560680
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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