A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573721



Internal ID16014444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89056331..89140075hg38UCSC Ensembl
Innerchr16:89122739..89206483hg19UCSC Ensembl
Innerchr16:87650240..87733984hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3883745
hg1983745
hg1883745
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149663
SamplesNINDS_51
Known GenesACSF3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573721
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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