A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3196609



Internal ID10869589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7229634..7229701hg38UCSC Ensembl
chr16:7279635..7279702hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv7466176
SamplesHuRef
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3196609
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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