A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204233



Internal ID20771273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8683501..8694200hg38UCSC Ensembl
chr21:9572334..9583033hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3810700
hg1910700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553150
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204233
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.28533


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