A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826687



Internal ID16120643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41136353..41200002hg38UCSC Ensembl
Innerchr14:41605556..41669205hg19UCSC Ensembl
Innerchr14:40675306..40738955hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3863650
hg1963650
hg1863650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564478
Supporting Variants
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv826687
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