A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481693



Internal ID21139246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76987119..76989875hg38UCSC Ensembl
chr14:77453462..77456218hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382757
hg192757
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021215
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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