A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431127



Internal ID21088680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86525025..86528074hg38UCSC Ensembl
chr8:87537253..87540302hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg383050
hg193050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170255
Samples
Known GenesCPNE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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