A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065657



Internal ID21974890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188180797..188180797hg38UCSC Ensembl
chr3:187898585..187898585hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38119
hg19119
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550535
Samples
Known GenesFLJ42393, LPP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065657
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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