A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909269



Internal ID22684479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132047646..132047698hg38UCSC Ensembl
chr10:133861150..133861202hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355565
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909269
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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