A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054056



Internal ID19143275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:66381516..66479417hg38UCSC Ensembl
Innerchr14:66848234..66946135hg19UCSC Ensembl
Innerchr14:65917987..66015888hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3897902
hg1997902
hg1897902
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531087, nssv3531086
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)nsv1054056
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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