A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083535



Internal ID21279819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40351713..40358449hg38UCSC Ensembl
Innerchr6:40319452..40326188hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg386737
hg196737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117648
Supporting Variants
Samplessample29
Known GenesLINC00951
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083535
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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