A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856689



Internal ID16150645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48384822..48385647hg38UCSC Ensembl
Innerchr16:48418733..48419558hg19UCSC Ensembl
Innerchr16:46976234..46977059hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38826
hg19826
hg18826
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572554
Supporting Variants
Samples
Known GenesMIR548AE2, SIAH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv856689
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer