A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571437



Internal ID16358846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:9304841..9315453hg38UCSC Ensembl
Innerchr16:9398698..9409310hg19UCSC Ensembl
Innerchr16:9306199..9316811hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3810613
hg1910613
hg1810613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852516
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571437
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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