A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571026



Internal ID16011749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:760143..810673hg38UCSC Ensembl
Innerchr16:810143..860673hg19UCSC Ensembl
Innerchr16:750144..800674hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3850531
hg1950531
hg1850531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4827n54
Supporting Variantsnssv851750
Samples
Known GenesCHTF18, GNG13, MIR662, MSLN, PRR25, RPUSD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571026
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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