A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223767



Internal ID20790807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63768068..63783927hg38UCSC Ensembl
chr8:64680626..64696484hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3815860
hg1915859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431598
Supporting Variants
Samples
Known GenesLOC286184
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223767
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00066


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