A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552588



Internal ID15993311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133257500..133333210hg38UCSC Ensembl
Innerchr10:135071004..135146714hg19UCSC Ensembl
Innerchr10:134920995..134996704hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3875711
hg1975711
hg1875710
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1475n54
Supporting Variantsnssv1174739
Samples1780862540_A
Known GenesADAM8, CALY, TUBGCP2, ZNF511
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552588
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