A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14102444



Internal ID21289492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:160155708..160188081hg38UCSC Ensembl
Innerchr2:161012219..161044592hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3832374
hg1932374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3111120
Supporting Variants
Samplessample47
Known GenesITGB6
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14102444
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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