A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450106



Internal ID21107659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65682334..65683109hg38UCSC Ensembl
chr10:67442092..67442867hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38776
hg19776
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982981
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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