A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563263



Internal ID16350672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113040195..113083861hg38UCSC Ensembl
Innerchr13:113694509..113738175hg19UCSC Ensembl
Innerchr13:112742510..112786176hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3843667
hg1943667
hg1843667
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3425n54
Supporting Variantsnssv820446
Samples
Known GenesMCF2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563263
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