A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637774



Internal ID6677875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6884336..6903888hg38UCSC Ensembl
chr16:6934337..6953889hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819553
hg1919553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365729, essv15365730
SamplesHG03237, HG02108
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637774
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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