A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059997



Internal ID19149216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:80175470..80213153hg38UCSC Ensembl
Innerchr16:80209367..80247050hg19UCSC Ensembl
Innerchr16:78766868..78804551hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3837684
hg1937684
hg1837684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719076
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059997
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