A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3213891



Internal ID22360697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12401141..12401317hg38UCSC Ensembl
chr10:12443140..12443316hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv802n152
Supporting Variantsnssv14330494, nssv14330496, nssv14330495
SamplesNA19238, NA19240, HG00513
Known GenesCAMK1D
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3213891
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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