A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421696



Internal ID21079249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:47978496..47983681hg38UCSC Ensembl
chr8:48891056..48896241hg19UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg385186
hg195186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167711
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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