A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050882



Internal ID19140101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8081699..8122226hg38UCSC Ensembl
Innerchr16:8131701..8172228hg19UCSC Ensembl
Innerchr16:8071702..8112229hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3840528
hg1940528
hg1840528
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2723n100
Supporting Variantsnssv3557099
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)nsv1050882
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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