A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543835



Internal ID20917076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:32379646..32387011hg38UCSC Ensembl
chr22:32775633..32782998hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg387366
hg197366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073779
Samples
Known GenesLOC339666
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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