A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549327



Internal ID20922489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:46491761..46492455hg38UCSC Ensembl
chr20:45120400..45121094hg19UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg38695
hg19695
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549327
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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