A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572693



Internal ID16013416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:55809206..55844051hg38UCSC Ensembl
Innerchr16:55843118..55877963hg19UCSC Ensembl
Innerchr16:54400619..54435464hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3834846
hg1934846
hg1834846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv857728
Samples
Known GenesCES1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572693
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