A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540899



Internal ID20914187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33691104..33712915hg38UCSC Ensembl
chr22:34087090..34108901hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3821812
hg1921812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073630
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540899
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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