A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5486576



Internal ID263937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43225043..43225123hg38UCSC Ensembl
chr10:43720491..43720571hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032743
Samples
Known GenesRASGEF1A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5486576
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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