A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834417



Internal ID16128373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104191423..104302812hg38UCSC Ensembl
Innerchr14:104657760..104769149hg19UCSC Ensembl
Innerchr14:103727513..103840194hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38111390
hg19111390
hg18112682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566032
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834417
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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