A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527560



Internal ID22396947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124306124..124306304hg38UCSC Ensembl
chr10:125994693..125994873hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1088n152
Supporting Variantsnssv14355256, nssv14355255
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527560
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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