A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6056109



Internal ID21965342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195537086..195537086hg38UCSC Ensembl
chr2:196401810..196401810hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg382091
hg192091
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534552
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6056109
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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