A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429694



Internal ID21087247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:121387601..121418300hg38UCSC Ensembl
chr8:122399841..122430540hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3830700
hg1930700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7481n223
Supporting Variantsnssv18220269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429694
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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