A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637737



Internal ID6677838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6015316..6111475hg38UCSC Ensembl
chr16:6065317..6161476hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3896160
hg1996160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv475e214
Supporting Variantsessv15364736, essv15364735, essv15364737
SamplesHG03943, NA19452, NA19434
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637737
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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