A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042414



Internal ID19131633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42415150..42685403hg38UCSC Ensembl
Innerchr14:42884353..43154606hg19UCSC Ensembl
Innerchr14:41954103..42224356hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38270254
hg19270254
hg18270254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3712299
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)nsv1042414
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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