A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425492



Internal ID21083045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:114935656..114936621hg38UCSC Ensembl
chr8:115947885..115948850hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg38966
hg19966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18163449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425492
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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