A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427065



Internal ID21084618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:86690401..86698200hg38UCSC Ensembl
chr8:87702629..87710428hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg387800
hg197800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229139
Samples
Known GenesCNGB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427065
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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