A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046399



Internal ID19135618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26369845..26392849hg38UCSC Ensembl
Innerchr14:26839051..26862055hg19UCSC Ensembl
Innerchr14:25908891..25931895hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3823005
hg1923005
hg1823005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1855n100
Supporting Variantsnssv3528541, nssv3528542, nssv3528544, nssv3528543
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)nsv1046399
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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