A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv860785



Internal ID16154741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77096442..77118437hg38UCSC Ensembl
Innerchr16:77130339..77152334hg19UCSC Ensembl
Innerchr16:75687840..75709835hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3821996
hg1921996
hg1821996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573122
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)nssv860785
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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