A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637741



Internal ID6677842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6151306..6207430hg38UCSC Ensembl
Innerchr16:6151306..6207430hg38UCSC Ensembl
Outerchr16:6150806..6207930hg38UCSC Ensembl
chr16:6201307..6257431hg19UCSC Ensembl
Innerchr16:6201307..6257431hg19UCSC Ensembl
Outerchr16:6200807..6257931hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3856125
hg1956125
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15364741
SamplesHG01672
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637741
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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