A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571773



Internal ID16359182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28603480..28610911hg38UCSC Ensembl
Innerchr16:28614801..28622232hg19UCSC Ensembl
Innerchr16:28522302..28529733hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387432
hg197432
hg187432
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4981n54
Supporting Variantsnssv855416
Samples
Known GenesSULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571773
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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