A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5425955



Internal ID204904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24068865..24068988hg38UCSC Ensembl
chr1:24395355..24395478hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16901168
Samples
Known GenesMYOM3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5425955
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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