A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571742



Internal ID16012465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28597166..28610911hg38UCSC Ensembl
Innerchr16:28608487..28622232hg19UCSC Ensembl
Innerchr16:28515988..28529733hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3813746
hg1913746
hg1813746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4971n54
Supporting Variantsnssv855273
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571742
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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