A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204118



Internal ID20771158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43786086..43839640hg38UCSC Ensembl
chr21:45205967..45259521hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3853555
hg1953555
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546862
Supporting Variants
Samples
Known GenesLOC284837, RRP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204118
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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