A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892796



Internal ID18836930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14961008..15074903hg38UCSC Ensembl
Outerchr16:14961008..15074903hg38UCSC Ensembl
Innerchr16:15054865..15168760hg19UCSC Ensembl
Outerchr16:15054865..15168760hg19UCSC Ensembl
Innerchr16:14962366..15076261hg18UCSC Ensembl
Outerchr16:14962366..15076261hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38113896
hg19113896
hg18113896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25799868
Samples
Known GenesMIR1972-1, MIR1972-2, NTAN1, PDXDC1, RRN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892796
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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