A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472186



Internal ID249902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16845153..16845243hg38UCSC Ensembl
chr5:16845262..16845352hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962106
Samples
Known GenesMYO10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472186
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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