A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637796



Internal ID6677897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7359827..7368897hg38UCSC Ensembl
Innerchr16:7360327..7368397hg38UCSC Ensembl
Outerchr16:7358827..7369897hg38UCSC Ensembl
chr16:7409828..7418898hg19UCSC Ensembl
Innerchr16:7410328..7418398hg19UCSC Ensembl
Outerchr16:7408828..7419898hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389071
hg199071
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15366878
SamplesNA20807
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637796
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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