A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423841



Internal ID21081394
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 StatusM
Merged Variants
Supporting Variantsnssv18169811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423841
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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