A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3215492



Internal ID22361806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59634711..59635108hg38UCSC Ensembl
chr11:59402184..59402581hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358972, nssv14358969, nssv14358973, nssv14358971, nssv14358970
SamplesHG00731, NA19240, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3215492
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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