A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168665



Internal ID20735705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:60247114..60248825hg38UCSC Ensembl
chr8:61159673..61161384hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg381712
hg191712
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419401
Supporting Variants
Samples
Known GenesCA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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