A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571779



Internal ID16012502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:28622897..28705218hg38UCSC Ensembl
Innerchr16:28634218..28716539hg19UCSC Ensembl
Innerchr16:28541719..28624040hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3882322
hg1982322
hg1882322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4972n54
Supporting Variantsnssv855423
Samples
Known GenesEIF3C, SULT1A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571779
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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