A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482804



Internal ID21140357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72789776..72802047hg38UCSC Ensembl
chr14:73256484..73268755hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3812272
hg1912272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021064
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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