A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204228



Internal ID20771268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:7224101..7231000hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg386900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554614
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204228
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00152


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