A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043480



Internal ID19132699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22155699..22478914hg38UCSC Ensembl
Innerchr14:22623632..22947903hg19UCSC Ensembl
Innerchr14:21693472..22017743hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38323216
hg19324272
hg18324272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1806n100
Supporting Variantsnssv3532205
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)nsv1043480
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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