A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450809



Internal ID21108362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68799701..68801800hg38UCSC Ensembl
chr10:70559458..70561557hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450809
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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