A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033100



Internal ID20600140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89187191..89189365hg38UCSC Ensembl
chr16:89253599..89255773hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382175
hg192175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503388
Supporting Variants
Samples
Known GenesCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033100
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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