A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149654



Internal ID15507224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:52434324..52488805hg38UCSC Ensembl
Innerchr16:52468236..52522717hg19UCSC Ensembl
Innerchr16:51025737..51080218hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3854482
hg1954482
hg1854482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572616
Supporting Variants
Samples1780854481_A
Known GenesTOX3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149654
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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