A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637787



Internal ID6677888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7011610..7048738hg38UCSC Ensembl
Innerchr16:7012110..7048238hg38UCSC Ensembl
Outerchr16:7010610..7049738hg38UCSC Ensembl
chr16:7061611..7098739hg19UCSC Ensembl
Innerchr16:7062111..7098239hg19UCSC Ensembl
Outerchr16:7060611..7099739hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3837129
hg1937129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365820, essv15365819, essv15365822, essv15365821
SamplesNA19091, HG03237, HG00311, HG00684
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637787
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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