A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054005



Internal ID21963239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3035045..3035045hg38UCSC Ensembl
chr2:3038817..3038817hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054005
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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