A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6040641



Internal ID21949980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:58614076..58614076hg38UCSC Ensembl
chr2:58841211..58841211hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527780
Samples
Known GenesLINC01122
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6040641
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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