A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559767



Internal ID21884122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154525802..154528303hg38UCSC Ensembl
chr6:154846936..154849437hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559767
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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