A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418861



Internal ID21076414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:75330667..75331355hg38UCSC Ensembl
chr8:76242902..76243590hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38689
hg19689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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