A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5404636



Internal ID183985
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68130703..68130754hg38UCSC Ensembl
chr10:69890460..69890511hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037400
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5404636
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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