A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573720



Internal ID16014443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88968841..89184474hg38UCSC Ensembl
Innerchr16:89035249..89250882hg19UCSC Ensembl
Innerchr16:87562750..87778383hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38215634
hg19215634
hg18215634
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863305
Samples
Known GenesACSF3, CBFA2T3, CDH15, LINC00304, LOC400558
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573720
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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