A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484781



Internal ID21142334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73413168..73413966hg38UCSC Ensembl
chr14:73879876..73880674hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020159
Samples
Known GenesNUMB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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