A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036063



Internal ID19125282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:43158036..43281136hg38UCSC Ensembl
Innerchr14:43627239..43750339hg19UCSC Ensembl
Innerchr14:42696989..42820089hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38123101
hg19123101
hg18123101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3530220
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)nsv1036063
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer