A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5599089



Internal ID21547722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24656213..24656937hg38UCSC Ensembl
chr10:24945142..24945866hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38725
hg19725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068175
SamplesNA19238
Known GenesARHGAP21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5599089
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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