A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6537689



Internal ID20911024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:36216892..36318217hg38UCSC Ensembl
chr22:36612938..36714262hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38101326
hg19101325
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204614
Samples
Known GenesAPOL1, APOL2, MIR6819, MYH9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6537689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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