A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043078



Internal ID19132297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18605720..19735727hg38UCSC Ensembl
Innerchr14:19382197..20203886hg19UCSC Ensembl
Innerchr14:18452197..19273726hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg381130008
hg19821690
hg18821530
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1759n100
Supporting Variantsnssv3526997
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H2, POTEG, POTEM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043078
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