A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546335



Internal ID20919553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:23400152..23401788hg38UCSC Ensembl
chr22:23742339..23743975hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381637
hg191637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073543
Samples
Known GenesZDHHC8P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546335
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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