A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573364



Internal ID16360773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81739604..81774628hg38UCSC Ensembl
Innerchr16:81773209..81808233hg19UCSC Ensembl
Innerchr16:80330710..80365734hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3835025
hg1935025
hg1835025
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149322
SamplesNINDS_74
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573364
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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