A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637745



Internal ID6677846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6392766..6425577hg38UCSC Ensembl
Innerchr16:6392777..6425567hg38UCSC Ensembl
Outerchr16:6392756..6425588hg38UCSC Ensembl
chr16:6442767..6475578hg19UCSC Ensembl
Innerchr16:6442778..6475568hg19UCSC Ensembl
Outerchr16:6442757..6475589hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3832812
hg1932812
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15364751
SamplesHG00978
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637745
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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