A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445837



Internal ID21103390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63544101..63644300hg38UCSC Ensembl
chr9:68139835..68240034hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38100200
hg19100200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7768n223
Supporting Variantsnssv18223388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445837
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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