A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202905



Internal ID20769945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46088601..46090100hg38UCSC Ensembl
chr20:44717240..44718739hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547714
Supporting Variants
Samples
Known GenesNCOA5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00024


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