A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv826661



Internal ID16120617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40444406..40461883hg38UCSC Ensembl
Innerchr14:40913610..40931087hg19UCSC Ensembl
Innerchr14:39983360..40000837hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3817478
hg1917478
hg1817478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564461
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)nssv826661
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