A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203891



Internal ID20770931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56638659..56641338hg38UCSC Ensembl
chr20:55213715..55216394hg19UCSC Ensembl
Cytoband20q13.31
Allele length
AssemblyAllele length
hg382680
hg192680
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6551587
Supporting Variants
Samples
Known GenesTFAP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203891
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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