A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067167



Internal ID18809698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88209906..88343034hg38UCSC Ensembl
Innerchr16:88243512..88376640hg19UCSC Ensembl
Innerchr16:86801013..86934141hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38133129
hg19133129
hg18133129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719124
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)nsv1067167
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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