A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051531



Internal ID18794062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:19004112..19117453hg38UCSC Ensembl
Innerchr16:19015434..19128775hg19UCSC Ensembl
Innerchr16:18922935..19036276hg18UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38113342
hg19113342
hg18113342
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3542771
Samples
Known GenesCOQ7, ITPRIPL2, TMC7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051531
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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