A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413143



Internal ID21070696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146918275..146920309hg38UCSC Ensembl
chr5:146297838..146299872hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382035
hg192035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126078
Samples
Known GenesPPP2R2B, PPP2R2B-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413143
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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