A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv855514



Internal ID16149470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32181960..33371260hg38UCSC Ensembl
Innerchr16:32193281..33272501hg19UCSC Ensembl
Innerchr16:32100782..33180002hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381189301
hg191079221
hg181079221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571835
Supporting Variants
Samples
Known GenesLOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv855514
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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