A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3221008



Internal ID22365535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119164041..119164283hg38UCSC Ensembl
chr10:120923553..120923795hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38243
hg19243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354433
SamplesHG00513
Known GenesSFXN4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3221008
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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