A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv561111



Internal ID16348520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:132687746..132688755hg38UCSC Ensembl
Innerchr12:133264332..133265341hg19UCSC Ensembl
Innerchr12:131774405..131775414hg18UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg381010
hg191010
hg181010
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3053n54
Supporting Variantsnssv805917
Samples
Known GenesPXMP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv561111
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