A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918971



Internal ID22694193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65652671..65654081hg38UCSC Ensembl
chr10:67412429..67413839hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381411
hg191411
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918971
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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