A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045932



Internal ID18788463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:18341508..19289336hg38UCSC Ensembl
Innerchr14:19117985..19877060hg19UCSC Ensembl
Innerchr14:18187985..18947060hg18UCSC Ensembl
Cytoband14q11.1
Allele length
AssemblyAllele length
hg38947829
hg19759076
hg18759076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1751n100
Supporting Variantsnssv3526899
Samples
Known GenesBMS1P17, BMS1P18, LOC642426, OR11H12, POTEG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045932
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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