A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14104270



Internal ID21289214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:185757024..185773816hg38UCSC Ensembl
Innerchr3:185474812..185491604hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg3816793
hg1916793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117341
Supporting Variants
Samplessample44
Known GenesIGF2BP2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14104270
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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