A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637790



Internal ID6677891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7028745..7038107hg38UCSC Ensembl
Innerchr16:7028745..7038107hg38UCSC Ensembl
Outerchr16:7028245..7038607hg38UCSC Ensembl
chr16:7078746..7088108hg19UCSC Ensembl
Innerchr16:7078746..7088108hg19UCSC Ensembl
Outerchr16:7078246..7088608hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389363
hg199363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365836, essv15365835, essv15365834
SamplesHG03237, HG00311, HG00684
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637790
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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