A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3529829



Internal ID18481424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105563288..105795460hg38UCSC Ensembl
Innerchr14:106029625..106261807hg19UCSC Ensembl
Innerchr14:105100670..105332852hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38232173
hg19232183
hg18232183
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039859
Supporting Variants
Samples
Known GenesELK2AP, MIR8071-1, MIR8071-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3529829
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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