A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562354



Internal ID16003077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:75635745..75636856hg38UCSC Ensembl
Innerchr13:76209881..76210992hg19UCSC Ensembl
Innerchr13:75107882..75108993hg18UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg381112
hg191112
hg181112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3258n54
Supporting Variantsnssv815775
Samples
Known GenesLMO7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562354
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