A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588606



Internal ID21780649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24655813..24655888hg38UCSC Ensembl
chr10:24944742..24944817hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6012973
Supporting Variants
Samples
Known GenesARHGAP21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588606
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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