A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5593096



Internal ID21541681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:93785720..93786713hg38UCSC Ensembl
chr10:95545477..95546470hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38994
hg19994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071575
SamplesHG00731
Known GenesLGI1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5593096
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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