A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18072893



Internal ID20639933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:19241022..19247226hg38UCSC Ensembl
chr22:19228545..19234749hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg386205
hg196205
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548305
Supporting Variants
Samples
Known GenesCLTCL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18072893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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