A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421567



Internal ID21079120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64278880..64296957hg38UCSC Ensembl
chr8:65191437..65209514hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3818078
hg1918078
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225452
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421567
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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