A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852269



Internal ID16146225
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 StatusS
Merged Variantsnsv571261
Supporting Variants
Samples
Known GenesCREBBP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852269
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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