A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571550



Internal ID16012273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:16152307..16168715hg38UCSC Ensembl
Innerchr16:16246164..16262572hg19UCSC Ensembl
Innerchr16:16153665..16170073hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3816409
hg1916409
hg1816409
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4927n54
Supporting Variantsnssv852828, nssv852829
Samples
Known GenesABCC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571550
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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