A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045368



Internal ID18787899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3340579..3375325hg38UCSC Ensembl
Innerchr16:3390579..3425325hg19UCSC Ensembl
Innerchr16:3330580..3365326hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3834747
hg1934747
hg1834747
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2694n100
Supporting Variantsnssv3556963
Samples
Known GenesMTRNR2L4, OR2C1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045368
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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