A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045403



Internal ID19134622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24780616..24802609hg38UCSC Ensembl
Innerchr14:25249822..25271815hg19UCSC Ensembl
Innerchr14:24319662..24341655hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3821994
hg1921994
hg1821994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528528, nssv3528529
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)nsv1045403
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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