A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25801185



Internal ID18834229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:6231292..6406762hg38UCSC Ensembl
Innerchr16:6281293..6456763hg19UCSC Ensembl
Innerchr16:6221294..6396764hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38175471
hg19175471
hg18175471
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892769
Supporting Variants
Samples
Known GenesRBFOX1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=91
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25801185
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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