A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066997



Internal ID19156216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22701658..22770637hg38UCSC Ensembl
Innerchr16:22712979..22781958hg19UCSC Ensembl
Innerchr16:22620480..22689459hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3868980
hg1968980
hg1868980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549119
Samples
Known GenesMIR548AA2, MIR548D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066997
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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