A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508151



Internal ID20881449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:101847748..101852554hg38UCSC Ensembl
chr14:102314085..102318891hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg384807
hg194807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015609
Samples
Known GenesPPP2R5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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