A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573842



Internal ID16014565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89964848..90038925hg38UCSC Ensembl
Innerchr16:90031256..90105333hg19UCSC Ensembl
Innerchr16:88558757..88632834hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3874078
hg1974078
hg1874078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv864028
Samples
Known GenesAFG3L1P, C16orf3, CENPBD1, DBNDD1, DEF8, GAS8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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