A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3217129



Internal ID22362886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:881582..881656hg38UCSC Ensembl
chr11:881582..881656hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1207n152
Supporting Variantsnssv14356455, nssv14356456
SamplesNA19239, NA19240
Known GenesCHID1
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3217129
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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