A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3117379



Internal ID21300645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:21206693..21229810hg38UCSC Ensembl
Innerchr6:21206924..21230041hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3823118
hg1923118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087780, nssv14082813
Samplessample237, sample6
Known GenesCDKAL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3117379
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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