A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3711394



Internal ID19009675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104322764..104449190hg38UCSC Ensembl
Innerchr14:104789101..104915527hg19UCSC Ensembl
Innerchr14:103860146..103986572hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38126427
hg19126427
hg18126427
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1054960
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)nssv3711394
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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