A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17589907



Internal ID21781950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48429563..48441811hg38UCSC Ensembl
chr10:49637606..49649854hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3812249
hg1912249
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6003687
Supporting Variants
Samples
Known GenesMAPK8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17589907
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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