A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3113580



Internal ID21296846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:167442492..167445644hg38UCSC Ensembl
Innerchr3:167160280..167163432hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg383153
hg193153
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14105902, nssv14108563, nssv14105367, nssv14105926, nssv14108139
Samplessample123, sample203, sample359, sample108, sample127
Known GenesSERPINI2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nsv3113580
Frequency
Sample Size467
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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