A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637764



Internal ID6677865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:6764326..6795417hg38UCSC Ensembl
Innerchr16:6764826..6794917hg38UCSC Ensembl
Outerchr16:6763326..6796417hg38UCSC Ensembl
chr16:6814327..6845418hg19UCSC Ensembl
Innerchr16:6814827..6844918hg19UCSC Ensembl
Outerchr16:6813327..6846418hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3831092
hg1931092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15365527, essv15365525, essv15365524, essv15365526, essv15365523
SamplesHG03237, HG00290, HG02332, NA20522, HG03196
Known GenesRBFOX1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637764
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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