A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5489006



Internal ID266298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68202825..68206078hg38UCSC Ensembl
chr10:69962582..69965835hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383254
hg193254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17037406
Samples
Known GenesMYPN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5489006
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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