A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449403



Internal ID21106956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131894354..131894656hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978509
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449403
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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