A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17042307



Internal ID95920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131938616..131939607hg38UCSC Ensembl
chr10:133752120..133753111hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6144040
Supporting Variants
Samples
Known GenesPPP2R2D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17042307
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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