A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3110216



Internal ID21293482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:71601403..71607171hg38UCSC Ensembl
Innerchr6:72311106..72316874hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg385769
hg195769
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14082860, nssv14087700
Samplessample216, sample299
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3110216
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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