A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv787415



Internal ID16081371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7869336..7938243hg38UCSC Ensembl
Innerchr12:8021932..8090839hg19UCSC Ensembl
Innerchr12:7913199..7982106hg18UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3868908
hg1968908
hg1868908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv557322
Supporting Variants
Samples
Known GenesSLC2A14, SLC2A3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv787415
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