A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481784



Internal ID21139337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:80249621..80250433hg38UCSC Ensembl
chr14:80715964..80716776hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021296
Samples
Known GenesDIO2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481784
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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