A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054248



Internal ID18796779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14956016..15014718hg38UCSC Ensembl
Innerchr16:15049873..15108575hg19UCSC Ensembl
Innerchr16:14957374..15016076hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3858703
hg1958703
hg1858703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2763n100
Supporting Variantsnssv3557840
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)nsv1054248
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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