A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6539737



Internal ID20913032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:43403764..43408990hg38UCSC Ensembl
chr22:43799770..43804996hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg385227
hg195227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074387
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6539737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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