A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563156



Internal ID16350565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914229..110915527hg38UCSC Ensembl
Innerchr13:111566576..111567874hg19UCSC Ensembl
Innerchr13:110364577..110365875hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg381299
hg191299
hg181299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3403n54
Supporting Variantsnssv819907, nssv819909, nssv819908
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563156
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