A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163781



Internal ID20730821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:117525108..117525544hg38UCSC Ensembl
chr8:118537347..118537783hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418310
Supporting Variants
Samples
Known GenesMED30
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00205


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