A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429533



Internal ID21087086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65528900..65532009hg38UCSC Ensembl
chr8:66441135..66444244hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg383110
hg193110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18169357
Samples
Known GenesLOC286186
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429533
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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