A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422400



Internal ID21079953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130912185..130979480hg38UCSC Ensembl
chr8:131924431..131991726hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3867296
hg1967296
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221147
Samples
Known GenesADCY8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422400
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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