A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083675



Internal ID21290131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:169064281..169065866hg38UCSC Ensembl
Innerchr6:169464376..169465961hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381586
hg191586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3112710
Supporting Variants
Samplessample56
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083675
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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