A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036298



Internal ID18778829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:15031584..15222857hg38UCSC Ensembl
Innerchr16:15125441..15316714hg19UCSC Ensembl
Innerchr16:15032942..15224215hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38191274
hg19191274
hg18191274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3557953
Samples
Known GenesMIR3180-4, MIR6511B-1, NTAN1, PDXDC1, RRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036298
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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