A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593639



Internal ID21542229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79506841..79506906hg38UCSC Ensembl
chr10:81266597..81266662hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071670
SamplesHG01114
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593639
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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