A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573745



Internal ID16361154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89783072..89809302hg38UCSC Ensembl
Innerchr16:89849480..89875710hg19UCSC Ensembl
Innerchr16:88376981..88403211hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3826231
hg1926231
hg1826231
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149669
SamplesHGDP01072
Known GenesFANCA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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