A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571315



Internal ID16012038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6047062..6064070hg38UCSC Ensembl
Innerchr16:6097063..6114071hg19UCSC Ensembl
Innerchr16:6037064..6054072hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817009
hg1917009
hg1817009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852355
Samples
Known GenesRBFOX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571315
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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