A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561150



Internal ID16348559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18469418..18729342hg38UCSC Ensembl
Innerchr13:19043558..19303482hg19UCSC Ensembl
Innerchr13:17941558..18201482hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38259925
hg19259925
hg18259925
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv805969
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561150
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer