A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561966



Internal ID16349375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63881032..64359486hg38UCSC Ensembl
Innerchr13:64455165..64933618hg19UCSC Ensembl
Innerchr13:63353166..63831619hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38478455
hg19478454
hg18478454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3203n54
Supporting Variantsnssv812603
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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