A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060851



Internal ID18803382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82146152..83643805hg38UCSC Ensembl
Innerchr16:82179757..83677410hg19UCSC Ensembl
Innerchr16:80737258..82234911hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg381497654
hg191497654
hg181497654
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3051n100
Supporting Variantsnssv3559849, nssv3559850
Samples
Known GenesCDH13, MIR3182, MIR8058, MPHOSPH6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060851
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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