A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002903



Internal ID21912246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48358074..48363983hg38UCSC Ensembl
chr10:49566117..49572026hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385910
hg195910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586777
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002903
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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