A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586147



Internal ID21534697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24656661..24656758hg38UCSC Ensembl
chr10:24945590..24945687hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17068176
SamplesHG00731
Known GenesARHGAP21
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586147
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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