A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040506



Internal ID18783037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14954899..15036113hg38UCSC Ensembl
Innerchr16:15048756..15129970hg19UCSC Ensembl
Innerchr16:14956257..15037471hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3881215
hg1981215
hg1881215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2764n100
Supporting Variantsnssv3557792
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)nsv1040506
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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