A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv856619



Internal ID16150575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:46419903..46466097hg38UCSC Ensembl
Innerchr16:46453815..46500009hg19UCSC Ensembl
Innerchr16:45011316..45057510hg18UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg3846195
hg1946195
hg1846195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv572517
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)nssv856619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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