A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571575



Internal ID16012298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:17272848..17292978hg38UCSC Ensembl
Innerchr16:17366705..17386835hg19UCSC Ensembl
Innerchr16:17274206..17294336hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3820131
hg1920131
hg1820131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852865
Samples
Known GenesXYLT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571575
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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