A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920630



Internal ID22695853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43816158..43829147hg38UCSC Ensembl
chr10:44311606..44324595hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3812990
hg1912990
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353512
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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