A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074162



Internal ID20641202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25885451..25885811hg38UCSC Ensembl
chr22:26281418..26281778hg19UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546437
Supporting Variants
Samples
Known GenesMYO18B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00111


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