A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061860



Internal ID21971093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170150136..170150136hg38UCSC Ensembl
chr5:169577140..169577140hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38237
hg19237
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061860
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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