A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6417720



Internal ID21075273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130979392..131685440hg38UCSC Ensembl
chr8:131991638..132697687hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38706049
hg19706050
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7494n223
Supporting Variantsnssv18236533
Samples
Known GenesADCY8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6417720
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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