A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17542958



Internal ID21867313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157156607..157156607hg38UCSC Ensembl
chr3:156874396..156874396hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6072672
Supporting Variants
Samples
Known GenesCCNL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17542958
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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