A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6044876



Internal ID21954154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:191154861..191154861hg38UCSC Ensembl
chr2:192019587..192019587hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38166
hg19166
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6044876
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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