A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073900



Internal ID20640940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:28746263..28763038hg38UCSC Ensembl
chr22:29142251..29159026hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3816776
hg1916776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6542443
Supporting Variants
Samples
Known GenesHSCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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