A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799868



Internal ID18830217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14961008..15074903hg38UCSC Ensembl
Innerchr16:15054865..15168760hg19UCSC Ensembl
Innerchr16:14962366..15076261hg18UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38113896
hg19113896
hg18113896
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892796
Supporting Variants
Samples
Known GenesMIR1972-1, MIR1972-2, NTAN1, PDXDC1, RRN3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=16
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799868
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer