A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529533



Internal ID20902894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14381008..14424978hg38UCSC Ensembl
chr20:14361654..14405624hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3843971
hg1943971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202189
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer