A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066896



Internal ID19156115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32269023..33908301hg38UCSC Ensembl
Innerchr16:32280344..33710768hg19UCSC Ensembl
Innerchr16:32187845..33618269hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381639279
hg191430425
hg181430425
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2844n100
Supporting Variantsnssv3550572, nssv3550573, nssv3550569, nssv3550570, nssv3550571
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066896
Frequency
Sample Size11257
Observed Gain4
Observed Loss1
Observed Complex0
Frequencyn/a


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