A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5426906



Internal ID205821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58679200..58679313hg38UCSC Ensembl
chr1:59144872..59144985hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16903420
Samples
Known GenesMYSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5426906
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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