A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3214163



Internal ID22360897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95324618..95324682hg38UCSC Ensembl
chr11:95057782..95057846hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1518n152
Supporting Variantsnssv14360125, nssv14360127, nssv14360126
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3214163
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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