A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546779



Internal ID20919989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33359964..33503028hg38UCSC Ensembl
chr22:33755950..33899014hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38143065
hg19143065
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073602
Samples
Known GenesLARGE, MIR4764
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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