A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552208



Internal ID16339617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115722372..115763827hg38UCSC Ensembl
Innerchr10:117481882..117523338hg19UCSC Ensembl
Innerchr10:117471872..117513328hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3841456
hg1941457
hg1841457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1401n54
Supporting Variantsnssv1175013
SamplesHGDP01185
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552208
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