A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563094



Internal ID16350503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:109784388..109787247hg38UCSC Ensembl
Innerchr13:110436735..110439594hg19UCSC Ensembl
Innerchr13:109234736..109237595hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg382860
hg192860
hg182860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819724
Samples
Known GenesIRS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563094
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