A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6548479



Internal ID20921665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:27110476..27111320hg38UCSC Ensembl
chr22:27506438..27507282hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38845
hg19845
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073201
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6548479
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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