A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510618



Internal ID287229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112467183..112467242hg38UCSC Ensembl
chr12:112904987..112905046hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17684558
Samples
Known GenesPTPN11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510618
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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