A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126079



Internal ID20693119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146919838..146926397hg38UCSC Ensembl
chr5:146299401..146305960hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg386560
hg196560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410172
Supporting Variants
Samples
Known GenesPPP2R2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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