A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551868



Internal ID16339277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89184902..89204638hg38UCSC Ensembl
Innerchr10:90944659..90964395hg19UCSC Ensembl
Innerchr10:90934639..90954375hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3819737
hg1919737
hg1819737
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1335n54
Supporting Variantsnssv753320
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551868
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