A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540935



Internal ID20914222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44586426..44593425hg38UCSC Ensembl
chr22:44982306..44989305hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074448
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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