A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563161



Internal ID16350570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:110914813..110918974hg38UCSC Ensembl
Innerchr13:111567160..111571321hg19UCSC Ensembl
Innerchr13:110365161..110369322hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg384162
hg194162
hg184162
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv819918, nssv819919
Samples
Known GenesANKRD10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563161
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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