A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206015



Internal ID20773055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25773231..25964092hg38UCSC Ensembl
chr21:27145542..27336405hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg38190862
hg19190864
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6554618
Supporting Variants
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206015
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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