A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489608



Internal ID21147161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72685970..72712380hg38UCSC Ensembl
chr14:73152678..73179088hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg3826411
hg1926411
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185710
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489608
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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