A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566209



Internal ID16006932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105465248..105475240hg38UCSC Ensembl
Innerchr14:105931585..105941577hg19UCSC Ensembl
Innerchr14:105002630..105012622hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg389993
hg199993
hg189993
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834809, nssv834808
Samples
Known GenesCRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566209
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer