A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565650



Internal ID16006373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:96623270..96659816hg38UCSC Ensembl
Innerchr14:97089607..97126153hg19UCSC Ensembl
Innerchr14:96159360..96195906hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3836547
hg1936547
hg1836547
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3867n54
Supporting Variantsnssv832730
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565650
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