A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206873



Internal ID20773913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34834163..35080409hg38UCSC Ensembl
chr2:35059230..35305475hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38246247
hg19246246
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343351
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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