A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561259



Internal ID16348668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:21951815..21976440hg38UCSC Ensembl
Innerchr13:22525954..22550579hg19UCSC Ensembl
Innerchr13:21423954..21448579hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3824626
hg1924626
hg1824626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv806195
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561259
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