A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481448



Internal ID21139001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80030063..80041320hg38UCSC Ensembl
chr14:80496406..80507663hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3811258
hg1911258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021011
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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