A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637783



Internal ID6677884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6984046..6990338hg38UCSC Ensembl
Innerchr16:6984069..6990316hg38UCSC Ensembl
Outerchr16:6984024..6990361hg38UCSC Ensembl
chr16:7034047..7040339hg19UCSC Ensembl
Innerchr16:7034070..7040317hg19UCSC Ensembl
Outerchr16:7034025..7040362hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg386293
hg196293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365809
SamplesHG02121
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637783
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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