A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561225



Internal ID16001948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:20238424..20456753hg38UCSC Ensembl
Innerchr13:20812563..21030892hg19UCSC Ensembl
Innerchr13:19710563..19928892hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg38218330
hg19218330
hg18218330
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3072n54
Supporting Variantsnssv806063
Samples
Known GenesCRYL1, MIR4499
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561225
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