A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559190



Internal ID21883545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:157505092..157507565hg38UCSC Ensembl
chr6:157926124..157928597hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg382474
hg192474
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012489
Supporting Variants
Samples
Known GenesZDHHC14
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559190
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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