A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525584



Internal ID21849942
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 StatusS
Merged Variantsnsv6054005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525584
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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