A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571187



Internal ID16011910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1974897..1980689hg38UCSC Ensembl
Innerchr16:2024898..2030690hg19UCSC Ensembl
Innerchr16:1964899..1970691hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385793
hg195793
hg185793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4860n54
Supporting Variantsnssv852080
Samples
Known GenesNOXO1, TBL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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