A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv801787



Internal ID15749057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:102407157..102413892hg38UCSC Ensembl
Innerchr12:102800935..102807670hg19UCSC Ensembl
Innerchr12:101325065..101331800hg18UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg386736
hg196736
hg186736
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv560035
Supporting Variants
Samples
Known GenesIGF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv801787
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