A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552211



Internal ID16339620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115808224..115842669hg38UCSC Ensembl
Innerchr10:117567735..117602180hg19UCSC Ensembl
Innerchr10:117557725..117592170hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3834446
hg1934446
hg1834446
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1175014
SamplesHGDP01063
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552211
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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