A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv830095



Internal ID16124051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:81707997..82195045hg38UCSC Ensembl
Innerchr14:82174341..82661389hg19UCSC Ensembl
Innerchr14:81244094..81731142hg18UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38487049
hg19487049
hg18487049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv565300
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)nssv830095
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