A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440373



Internal ID21097926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25643363..25851083hg38UCSC Ensembl
chr11:25664909..25872630hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38207721
hg19207722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1006n223
Supporting Variantsnssv17990056
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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