A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430307



Internal ID21087860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87366899..87398087hg38UCSC Ensembl
chr8:88379127..88410315hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3831189
hg1931189
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236635
Samples
Known GenesCNBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430307
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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