A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573796



Internal ID16014519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852186..89852857hg38UCSC Ensembl
Innerchr16:89918594..89919265hg19UCSC Ensembl
Innerchr16:88446095..88446766hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38672
hg19672
hg18672
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5333n54
Supporting Variantsnssv863610, nssv863612, nssv863611
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573796
Frequency
Sample Size17421
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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