A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422483



Internal ID21080036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103496516..103497586hg38UCSC Ensembl
chr8:104508744..104509814hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg381071
hg191071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162628
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422483
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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