A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3534382



Internal ID18832663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:106779223..106877229hg38UCSC Ensembl
Innerchr14:107187462..107285437hg19UCSC Ensembl
Innerchr14:106258507..106356482hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3898007
hg1997976
hg1897976
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039613
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3534382
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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