A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062836



Internal ID19152055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84582619..84612845hg38UCSC Ensembl
Innerchr16:84616225..84646451hg19UCSC Ensembl
Innerchr16:83173726..83203952hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3830227
hg1930227
hg1830227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3058n100
Supporting Variantsnssv3559959
Samples
Known GenesCOTL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062836
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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