A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573812



Internal ID16014535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89906008..89908560hg38UCSC Ensembl
Innerchr16:89972416..89974968hg19UCSC Ensembl
Innerchr16:88499917..88502469hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382553
hg192553
hg182553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863693, nssv863692, nssv863697, nssv863694, nssv863696, nssv863695
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573812
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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