A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914352



Internal ID22689569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133369344..133369443hg38UCSC Ensembl
chr10:135182848..135182947hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352653
Samples
Known GenesECHS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914352
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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