A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910882



Internal ID22686094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121034675..121034834hg38UCSC Ensembl
chr10:122794188..122794347hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351839
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910882
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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