A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543347



Internal ID20916596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:35353055..35367180hg38UCSC Ensembl
chr22:35749048..35763173hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg3814126
hg1914126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18074184
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543347
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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