A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5592660



Internal ID21541243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:111431790..111432099hg38UCSC Ensembl
chr10:113191548..113191857hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068500
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5592660
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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