A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205342



Internal ID20772382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:18451468..18452455hg38UCSC Ensembl
chr2:18632734..18633721hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg38988
hg19988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344179
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205342
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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