A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572709



Internal ID16013432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:57092295..57093081hg38UCSC Ensembl
Innerchr16:57126207..57126993hg19UCSC Ensembl
Innerchr16:55683708..55684494hg18UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38787
hg19787
hg18787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5139n54
Supporting Variantsnssv857761
Samples
Known GenesCPNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572709
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