A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778562



Internal ID15725832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:67141279..67149205hg38UCSC Ensembl
Innerchr11:66908750..66916676hg19UCSC Ensembl
Innerchr11:66665326..66673252hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387927
hg197927
hg187927
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555250
Supporting Variants
Samples
Known GenesKDM2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778562
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