A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563174



Internal ID16350583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:111029653..111107171hg38UCSC Ensembl
Innerchr13:111682000..111759518hg19UCSC Ensembl
Innerchr13:110480001..110557519hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3877519
hg1977519
hg1877519
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3405n54
Supporting Variantsnssv819935
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563174
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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