A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220504



Internal ID20787544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:144687575..144884662hg38UCSC Ensembl
chr8:145912960..146110047hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38197088
hg19197088
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429650
Supporting Variants
Samples
Known GenesCOMMD5, MIR6850, RPL8, ZNF250, ZNF251, ZNF34, ZNF517, ZNF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220504
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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