A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573801



Internal ID16014524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852237..89852755hg38UCSC Ensembl
Innerchr16:89918645..89919163hg19UCSC Ensembl
Innerchr16:88446146..88446664hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38519
hg19519
hg18519
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5333n54
Supporting Variantsnssv863667, nssv863665, nssv863666
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573801
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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