A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531674



Internal ID18829955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:46684126..46758334hg38UCSC Ensembl
Innerchr14:47153329..47227537hg19UCSC Ensembl
Innerchr14:46223079..46297287hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg3874209
hg1974209
hg1874209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047429
Supporting Variants
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)nssv3531674
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