A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562785



Internal ID16003508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:96090080..96090785hg38UCSC Ensembl
Innerchr13:96742334..96743039hg19UCSC Ensembl
Innerchr13:95540335..95541040hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38706
hg19706
hg18706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3328n54
Supporting Variantsnssv817563
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562785
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