A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563155



Internal ID16350564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914065..110915799hg38UCSC Ensembl
Innerchr13:111566412..111568146hg19UCSC Ensembl
Innerchr13:110364413..110366147hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381735
hg191735
hg181735
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3404n54
Supporting Variantsnssv819902, nssv819905, nssv819904, nssv819906, nssv819903
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563155
Frequency
Sample Size17421
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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