A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv862000



Internal ID16155956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:84008053..84047164hg38UCSC Ensembl
Innerchr16:84041658..84080769hg19UCSC Ensembl
Innerchr16:82599159..82638270hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3839112
hg1939112
hg1839112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv573420
Supporting Variants
Samples
Known GenesSLC38A8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv862000
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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