A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552590



Internal ID16339999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133268842..133281904hg38UCSC Ensembl
Innerchr10:135082346..135095408hg19UCSC Ensembl
Innerchr10:134932336..134945398hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3813063
hg1913063
hg1813063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762204
Samples
Known GenesADAM8, TUBGCP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552590
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