A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040791



Internal ID19130010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:55935209..55958113hg38UCSC Ensembl
Innerchr14:56401927..56424831hg19UCSC Ensembl
Innerchr14:55471680..55494584hg18UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg3822905
hg1922905
hg1822905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1921n100
Supporting Variantsnssv3531030
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)nsv1040791
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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