A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206308



Internal ID20773348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:56046944..56091549hg38UCSC Ensembl
chr2:56274079..56318684hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3844606
hg1944606
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6339174
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206308
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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