A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567433



Internal ID21759476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157310365..157314362hg38UCSC Ensembl
chr6:157731397..157735394hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg383998
hg193998
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017725
Supporting Variants
Samples
Known GenesTMEM242
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567433
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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