A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591559



Internal ID21540135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:89142617..89142667hg38UCSC Ensembl
chr10:90902374..90902424hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071769
SamplesHG01596
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591559
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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