A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066288



Internal ID18808819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:51074326..51139648hg38UCSC Ensembl
Innerchr16:51108237..51173559hg19UCSC Ensembl
Innerchr16:49665738..49731060hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3865323
hg1965323
hg1865323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3722706
Samples
Known GenesSALL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066288
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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