A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534688



Internal ID21859043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:28431312..28431312hg38UCSC Ensembl
chr2:28654179..28654179hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054780
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534688
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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