A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217029



Internal ID22362825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43146985..43147783hg38UCSC Ensembl
chr10:43642433..43643231hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38799
hg19799
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14343365
SamplesNA19240
Known GenesCSGALNACT2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217029
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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