A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552722



Internal ID15993445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133522014..133529663hg38UCSC Ensembl
Innerchr10:135335518..135343167hg19UCSC Ensembl
Innerchr10:135185508..135193157hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg387650
hg197650
hg187650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv762999
Samples
Known GenesCYP2E1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552722
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