A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571835



Internal ID16359244
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 StatusM
Merged Variants
Supporting Variantsnssv855514
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)nsv571835
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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