A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637780



Internal ID6677881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6909556..6939221hg38UCSC Ensembl
chr16:6959557..6989222hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3829666
hg1929666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365803, essv15365802, essv15365804
SamplesHG03237, NA20507, HG03785
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637780
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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