A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571261



Internal ID16011984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3878214..3880926hg38UCSC Ensembl
Innerchr16:3928215..3930927hg19UCSC Ensembl
Innerchr16:3868216..3870928hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382713
hg192713
hg182713
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852269
Samples
Known GenesCREBBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571261
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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