A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217050



Internal ID22362837
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14335799, nssv14335800, nssv14335798
SamplesNA19238, NA19239, NA19240
Known GenesARHGAP21
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217050
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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