A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564812



Internal ID16352221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48106920..48140672hg38UCSC Ensembl
Innerchr14:48576123..48609875hg19UCSC Ensembl
Innerchr14:47645873..47679625hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3833753
hg1933753
hg1833753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3711n54
Supporting Variantsnssv827841
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564812
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