A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3222321



Internal ID22366430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124876603..124876793hg38UCSC Ensembl
chr10:126565172..126565362hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1092n152
Supporting Variantsnssv14355905, nssv14355906, nssv14355904
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3222321
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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