A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046771



Internal ID18789302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954899..15031584hg38UCSC Ensembl
Innerchr16:15048756..15125441hg19UCSC Ensembl
Innerchr16:14956257..15032942hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3876686
hg1976686
hg1876686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2763n100
Supporting Variantsnssv3557789, nssv3557788, nssv3557791, nssv3557787, nssv3557790
Samples
Known GenesMIR1972-1, MIR1972-2, PDXDC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046771
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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