A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563381



Internal ID16350790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113886735..113936052hg38UCSC Ensembl
Innerchr13:114589708..114639025hg19UCSC Ensembl
Innerchr13:113474918..113524235hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3849318
hg1949318
hg1849318
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv820675
Samples
Known GenesLINC00452, LINC00565
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563381
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