A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074143



Internal ID20641183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25446715..25642171hg38UCSC Ensembl
chr22:25842682..26038138hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38195457
hg19195457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536174
Supporting Variants
Samples
Known GenesADRBK2, CRYBB2P1, MIR6817
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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