A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573794



Internal ID16014517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89852186..89852755hg38UCSC Ensembl
Innerchr16:89918594..89919163hg19UCSC Ensembl
Innerchr16:88446095..88446664hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38570
hg19570
hg18570
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5333n54
Supporting Variantsnssv863606, nssv863602, nssv863596, nssv863598, nssv863597, nssv863605, nssv863604, nssv863603, nssv863599, nssv863607, nssv863600, nssv863601, nssv863595
Samples
Known GenesSPIRE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573794
Frequency
Sample Size17421
Observed Gain6
Observed Loss7
Observed Complex0
Frequencyn/a


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