A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540328



Internal ID20913618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44220531..44235622hg38UCSC Ensembl
chr22:44616411..44631502hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3815092
hg1915092
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074435
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540328
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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