A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573798



Internal ID16014521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852186..89853617hg38UCSC Ensembl
Innerchr16:89918594..89920025hg19UCSC Ensembl
Innerchr16:88446095..88447526hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381432
hg191432
hg181432
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863659, nssv863660
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573798
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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