A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202157



Internal ID20769197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:10796269..10797623hg38UCSC Ensembl
chr20:10776917..10778271hg19UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg381355
hg191355
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6528542
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202157
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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