A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057666



Internal ID19146885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..33805240hg38UCSC Ensembl
Innerchr16:32180774..33607707hg19UCSC Ensembl
Innerchr16:32088275..33515208hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381635788
hg191426934
hg181426934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2842n100
Supporting Variantsnssv3550382
Samples
Known GenesLOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057666
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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