A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042555



Internal ID18785086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14964489..15014718hg38UCSC Ensembl
Innerchr16:15058346..15108575hg19UCSC Ensembl
Innerchr16:14965847..15016076hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3850230
hg1950230
hg1850230
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2767n100
Supporting Variantsnssv3557928
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)nsv1042555
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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