A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554790



Internal ID20927881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45043838..45059919hg38UCSC Ensembl
chr22:45439719..45455800hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3816082
hg1916082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4728n223
Supporting Variantsnssv18207559
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554790
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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