A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6551587



Internal ID20924720
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 StatusM
Merged Variants
Supporting Variantsnssv18203891
Samples
Known GenesTFAP2C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6551587
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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