A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480813



Internal ID21138366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:73865228..73897211hg38UCSC Ensembl
chr14:74331931..74363914hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3831984
hg1931984
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196817
Samples
Known GenesPTGR2, ZNF410
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480813
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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