A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573841



Internal ID16014564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89957794..90083514hg38UCSC Ensembl
Innerchr16:90024202..90149922hg19UCSC Ensembl
Innerchr16:88551703..88677423hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38125721
hg19125721
hg18125721
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149670
SamplesHGDP00460
Known GenesAFG3L1P, C16orf3, CENPBD1, DBNDD1, DEF8, GAS8, PRDM7, URAHP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573841
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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