A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6057506



Internal ID21966739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:23381416..23381416hg38UCSC Ensembl
chr2:23604287..23604287hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38143
hg19143
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6057506
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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