A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510141



Internal ID20883457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:90321569..90329856hg38UCSC Ensembl
chr14:90787913..90796200hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg388288
hg198288
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189417
Samples
Known GenesNRDE2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510141
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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