A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426618



Internal ID21084171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:111361532..111417820hg38UCSC Ensembl
chr8:112373761..112430049hg19UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3856289
hg1956289
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7459n223
Supporting Variantsnssv18226688
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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