A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551843



Internal ID16339252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:89066495..89114711hg38UCSC Ensembl
Innerchr10:90826252..90874468hg19UCSC Ensembl
Innerchr10:90816232..90864448hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3848217
hg1948217
hg1848217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753226
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551843
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