A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789881



Internal ID15737151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:27495478..27501548hg38UCSC Ensembl
Innerchr12:27648411..27654481hg19UCSC Ensembl
Innerchr12:27539678..27545748hg18UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg386071
hg196071
hg186071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557810
Supporting Variants
Samples
Known GenesSMCO2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789881
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