A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv773216



Internal ID15720486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:47331947..47342576hg38UCSC Ensembl
Innerchr11:47353498..47364127hg19UCSC Ensembl
Innerchr11:47310074..47320703hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3810630
hg1910630
hg1810630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554209
Supporting Variants
Samples
Known GenesMYBPC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv773216
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