A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428778



Internal ID21086331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:82054499..82396219hg38UCSC Ensembl
chr8:82966734..83308454hg19UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38341721
hg19341721
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229754
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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