A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6546707



Internal ID20919917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:33502301..33504300hg38UCSC Ensembl
chr22:33898287..33900286hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18073620
Samples
Known GenesLARGE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6546707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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