A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14335798



Internal ID22257488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:24645586..24651767hg38UCSC Ensembl
chr10:24934515..24940696hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386182
hg196182
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3217050
Supporting Variants
SamplesNA19238
Known GenesARHGAP21
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14335798
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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