A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573474



Internal ID16360883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:85090156..85114027hg38UCSC Ensembl
Innerchr16:85123762..85147633hg19UCSC Ensembl
Innerchr16:83681263..83705134hg18UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg3823872
hg1923872
hg1823872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv862188
Samples
Known GenesFAM92B, KIAA0513
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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