A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572908



Internal ID16013631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:68564104..68890598hg38UCSC Ensembl
Innerchr16:68598007..68924501hg19UCSC Ensembl
Innerchr16:67155508..67482002hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38326495
hg19326495
hg18326495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149186
SamplesHGDP00512
Known GenesCDH1, CDH3, TANGO6, ZFP90
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572908
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