A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423446



Internal ID21080999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59995144..60005825hg38UCSC Ensembl
chr8:60907703..60918384hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3810682
hg1910682
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169768
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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