A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037883



Internal ID20604923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65945901..65948100hg38UCSC Ensembl
chr17:63942019..63944218hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534813
Supporting Variants
Samples
Known GenesCEP112
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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