A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv798860



Internal ID16092816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:74456903..74494320hg38UCSC Ensembl
Innerchr12:74850683..74888100hg19UCSC Ensembl
Innerchr12:73136950..73174367hg18UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg3837418
hg1937418
hg1837418
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559415
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv798860
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