A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711404



Internal ID18662999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105612353..105806924hg38UCSC Ensembl
Innerchr14:106078690..106273250hg19UCSC Ensembl
Innerchr14:105149735..105344295hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38194572
hg19194561
hg18194561
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052262
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)nssv3711404
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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