A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203425



Internal ID20770465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:62937201..62938800hg38UCSC Ensembl
chr20:61568553..61570152hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540637
Supporting Variants
Samples
Known GenesDIDO1, GID8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203425
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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