A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049674



Internal ID19138893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:26286641..26315707hg38UCSC Ensembl
Innerchr14:26755847..26784913hg19UCSC Ensembl
Innerchr14:25825687..25854753hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3829067
hg1929067
hg1829067
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3528535, nssv3528536
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)nsv1049674
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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