A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417692



Internal ID21075245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:96217510..96239195hg38UCSC Ensembl
chr8:97229738..97251423hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3821686
hg1921686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220036
Samples
Known GenesUQCRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417692
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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