A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116616



Internal ID21299882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:40794936..40814384hg38UCSC Ensembl
Innerchr6:40762675..40782123hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3819449
hg1919449
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14087695
Samplessample214
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116616
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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