A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057720



Internal ID21966953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:179866776..179866776hg38UCSC Ensembl
chr2:180731503..180731503hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057720
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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