A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856199



Internal ID16150155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:34939284..34959533hg38UCSC Ensembl
Innerchr16:34173678..34193904hg19UCSC Ensembl
Innerchr16:34031179..34051405hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3820250
hg1920227
hg1820227
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572358
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)nssv856199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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