A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14108717



Internal ID21286328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:157500067..157501728hg38UCSC Ensembl
Innerchr3:157217856..157219517hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg381662
hg191662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117235
Supporting Variants
Samplessample386
Known GenesVEPH1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14108717
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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