A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800606



Internal ID18835382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:7012444..7019055hg38UCSC Ensembl
Innerchr16:7062445..7069056hg19UCSC Ensembl
Innerchr16:7002446..7009057hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg386612
hg196612
hg186612
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892773
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800606
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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