A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108139



Internal ID21274225
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 StatusS
Merged Variantsnsv3113580
Supporting Variants
Samplessample203
Known GenesSERPINI2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108139
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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