A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552209



Internal ID16339618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:115724951..115771644hg38UCSC Ensembl
Innerchr10:117484461..117531155hg19UCSC Ensembl
Innerchr10:117474451..117521145hg18UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3846694
hg1946695
hg1846695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1401n54
Supporting Variantsnssv758790
Samples
Known GenesATRNL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552209
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