A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527357



Internal ID20900718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:14122640..14211237hg38UCSC Ensembl
chr20:14103286..14191883hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3888598
hg1988598
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202186
Samples
Known GenesMACROD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527357
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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