A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861925



Internal ID16155881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81035712..81036505hg38UCSC Ensembl
Innerchr16:81069317..81070110hg19UCSC Ensembl
Innerchr16:79626818..79627611hg18UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38794
hg19794
hg18794
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573344
Supporting Variants
Samples
Known GenesATMIN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861925
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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