A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089392



Internal ID20656432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:47305929..47307710hg38UCSC Ensembl
chr2:47533068..47534849hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381782
hg191782
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6344772
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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