A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573527



Internal ID16360936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:86519041..86528307hg38UCSC Ensembl
Innerchr16:86552647..86561913hg19UCSC Ensembl
Innerchr16:85110148..85119414hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg389267
hg199267
hg189267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862316
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573527
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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