A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536055



Internal ID20909408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:42291053..42310311hg38UCSC Ensembl
chr22:42687059..42706317hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3819259
hg1919259
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207445
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536055
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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