A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571444



Internal ID16012167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10210433..10319015hg38UCSC Ensembl
Innerchr16:10304290..10412872hg19UCSC Ensembl
Innerchr16:10211791..10320373hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38108583
hg19108583
hg18108583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852523
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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