A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637791



Internal ID6677892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7036895..7042063hg38UCSC Ensembl
Innerchr16:7036916..7042042hg38UCSC Ensembl
Outerchr16:7036874..7042084hg38UCSC Ensembl
chr16:7086896..7092064hg19UCSC Ensembl
Innerchr16:7086917..7092043hg19UCSC Ensembl
Outerchr16:7086875..7092085hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385169
hg195169
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365838, essv15365839, essv15365837
SamplesHG01608, HG03237, HG00684
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637791
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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