A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209820



Internal ID20776861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46548771..46563099hg38UCSC Ensembl
chr2:46775910..46790238hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3814329
hg1914329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353072
Supporting Variants
Samples
Known GenesRHOQ
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209820
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00043


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