A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564624



Internal ID16352033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42863867..42895899hg38UCSC Ensembl
Innerchr14:43333070..43365102hg19UCSC Ensembl
Innerchr14:42402820..42434852hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3832033
hg1932033
hg1832033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv827509
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564624
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