A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476265



Internal ID253878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17745612..17752614hg38UCSC Ensembl
chr10:17787611..17794613hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg387003
hg197003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17030452
Samples
Known GenesTMEM236
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476265
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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