A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637781



Internal ID6677882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6928132..6984510hg38UCSC Ensembl
Innerchr16:6928132..6984510hg38UCSC Ensembl
Outerchr16:6927632..6985010hg38UCSC Ensembl
chr16:6978133..7034511hg19UCSC Ensembl
Innerchr16:6978133..7034511hg19UCSC Ensembl
Outerchr16:6977633..7035011hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856379
hg1956379
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365806, essv15365805
SamplesHG03237, HG00311
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637781
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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