A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3116932



Internal ID21300198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:19072487..19451119hg38UCSC Ensembl
Innerchr5:19072596..19451228hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38378633
hg19378633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv968n145
Supporting Variantsnssv14109244
Samplessample283
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3116932
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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