A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548503



Internal ID20921689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35438450..35438683hg38UCSC Ensembl
chr22:35834443..35834676hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074191
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548503
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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