A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736072



Internal ID20512017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24656650..24656756hg38UCSC Ensembl
chr10:24945579..24945685hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282290
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736072
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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