A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3111032



Internal ID21294298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:157821506..157826575hg38UCSC Ensembl
Innerchr6:158242538..158247607hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg385070
hg195070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14086403
Samplessample138
Known GenesSNX9
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3111032
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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