A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529799



Internal ID22399190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:100991975..100992286hg38UCSC Ensembl
chr10:102751732..102752043hg19UCSC Ensembl
Cytoband10q24.31
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352957
SamplesNA19239
Known GenesC10orf2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529799
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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