A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861940



Internal ID15809210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81724858..81746960hg38UCSC Ensembl
Innerchr16:81758463..81780565hg19UCSC Ensembl
Innerchr16:80315964..80338066hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3822103
hg1922103
hg1822103
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573363
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861940
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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