A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525697



Internal ID18477292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18225635..19014957hg38UCSC Ensembl
Innerchr14:19002112..19602662hg19UCSC Ensembl
Innerchr14:18072112..18672662hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38789323
hg19600551
hg18600551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048651
Supporting Variants
Samples
Known GenesLOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525697
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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