A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv789868



Internal ID15737138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:25206907..25244348hg38UCSC Ensembl
Innerchr12:25359841..25397282hg19UCSC Ensembl
Innerchr12:25251108..25288549hg18UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg3837442
hg1937442
hg1837442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557798
Supporting Variants
Samples
Known GenesKRAS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv789868
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