A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489634



Internal ID21147187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63463094..63465481hg38UCSC Ensembl
chr14:63929812..63932199hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg382388
hg192388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020631
Samples
Known GenesPPP2R5E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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