A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453106



Internal ID21110659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26580070..26643467hg38UCSC Ensembl
chr10:26868999..26932396hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3863398
hg1963398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv660n223
Supporting Variantsnssv17981177
Samples
Known GenesLINC00202-2, LINC00264
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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