A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18204100



Internal ID20771140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42831534..42847739hg38UCSC Ensembl
chr21:44251644..44267849hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3816206
hg1916206
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6544530
Supporting Variants
Samples
Known GenesWDR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18204100
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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