A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563365



Internal ID16004088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113398273..113400011hg38UCSC Ensembl
Innerchr13:114052588..114054326hg19UCSC Ensembl
Innerchr13:113100589..113102327hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381739
hg191739
hg181739
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3447n54
Supporting Variantsnssv820656, nssv820655, nssv820657
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563365
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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