A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282290



Internal ID20491508
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 StatusS
Merged Variantsnsv4736072
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282290
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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