A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059111



Internal ID19148330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:72613670..72718008hg38UCSC Ensembl
Innerchr16:72647569..72751907hg19UCSC Ensembl
Innerchr16:71205070..71309408hg18UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38104339
hg19104339
hg18104339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559572
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059111
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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