A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166482



Internal ID20733522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:138778964..138796655hg38UCSC Ensembl
chr8:139791207..139808898hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3817692
hg1917692
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428049
Supporting Variants
Samples
Known GenesCOL22A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166482
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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