A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536261



Internal ID20909614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:48985101..49054900hg38UCSC Ensembl
chr22:49380913..49450712hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3869800
hg1969800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536261
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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