A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053926



Internal ID19143145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19933041..19954541hg38UCSC Ensembl
Innerchr16:19944363..19965863hg19UCSC Ensembl
Innerchr16:19851864..19873364hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3821501
hg1921501
hg1821501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2789n100
Supporting Variantsnssv3542862, nssv3542863, nssv3542860, nssv3542859, nssv3542861, nssv3542864
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)nsv1053926
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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