A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573810



Internal ID16014533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89857498..90037251hg38UCSC Ensembl
Innerchr16:89923906..90103659hg19UCSC Ensembl
Innerchr16:88451407..88631160hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38179754
hg19179754
hg18179754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863689
Samples
Known GenesAFG3L1P, C16orf3, CENPBD1, DBNDD1, DEF8, GAS8, MC1R, SPIRE2, TCF25, TUBB3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573810
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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