A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827893



Internal ID16121849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:54232948..54246578hg38UCSC Ensembl
Innerchr14:54699666..54713296hg19UCSC Ensembl
Innerchr14:53769416..53783046hg18UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3813631
hg1913631
hg1813631
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564849
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)nssv827893
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