A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561817



Internal ID16349226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:57791755..57799534hg38UCSC Ensembl
Innerchr13:58365889..58373668hg19UCSC Ensembl
Innerchr13:57263890..57271669hg18UCSC Ensembl
Cytoband13q21.1
Allele length
AssemblyAllele length
hg387780
hg197780
hg187780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3174n54
Supporting Variantsnssv812154, nssv812153
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561817
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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