A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066385



Internal ID19155604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32217659..32473866hg38UCSC Ensembl
Innerchr16:32228980..32485187hg19UCSC Ensembl
Innerchr16:32136481..32392688hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38256208
hg19256208
hg18256208
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2855n100
Supporting Variantsnssv3550420
Samples
Known GenesLOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066385
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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