A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3212844



Internal ID22359969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131865835..131865970hg38UCSC Ensembl
chr11:131735729..131735864hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1639n152
Supporting Variantsnssv14362975, nssv14362976, nssv14362977, nssv14362978, nssv14362979, nssv14362974
SamplesNA19238, HG00731, NA19240, HG00733, HG00513, HG00514
Known GenesNTM
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3212844
Frequency
Sample Size9
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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