A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6545555



Internal ID20918786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63307491..63324904hg38UCSC Ensembl
chr20:61938843..61956256hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3817414
hg1917414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203434
Samples
Known GenesCOL20A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6545555
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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