A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169811



Internal ID20736851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63357940..63368532hg38UCSC Ensembl
chr8:64270498..64281090hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3810593
hg1910593
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423841
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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