A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491547



Internal ID21149100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:72802185..72803850hg38UCSC Ensembl
chr14:73268893..73270558hg19UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381666
hg191666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177311
Samples
Known GenesDPF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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