A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064331



Internal ID18806862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:69990674..70105639hg38UCSC Ensembl
Innerchr16:70024577..70139542hg19UCSC Ensembl
Innerchr16:68582078..68697043hg18UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38114966
hg19114966
hg18114966
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3001n100
Supporting Variantsnssv3559467, nssv3559466
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC2P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064331
Frequency
Sample Size29084
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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