A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573811



Internal ID16014534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89906008..89908228hg38UCSC Ensembl
Innerchr16:89972416..89974636hg19UCSC Ensembl
Innerchr16:88499917..88502137hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg382221
hg192221
hg182221
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv863690, nssv863691
Samples
Known GenesTCF25
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573811
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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