A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv861996



Internal ID15809266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83966212..84001017hg38UCSC Ensembl
Innerchr16:83999817..84034622hg19UCSC Ensembl
Innerchr16:82557318..82592123hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3834806
hg1934806
hg1834806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573411
Supporting Variants
Samples
Known GenesNECAB2, OSGIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv861996
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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