A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536969



Internal ID20910313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:12030001..12062500hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3832500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4617n223
Supporting Variantsnssv18203840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536969
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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