A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799387



Internal ID18828484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6849889..6872577hg38UCSC Ensembl
Innerchr16:6899890..6922578hg19UCSC Ensembl
Innerchr16:6839891..6862579hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3822689
hg1922689
hg1822689
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892775
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799387
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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