A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411352



Internal ID21068905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146599280..146599798hg38UCSC Ensembl
chr5:145978843..145979361hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126058
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411352
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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