A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643541



Internal ID6683612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5831170..5844611hg38UCSC Ensembl
Innerchr19:5831170..5844611hg38UCSC Ensembl
Outerchr19:5830670..5845111hg38UCSC Ensembl
chr19:5831181..5844622hg19UCSC Ensembl
Innerchr19:5831181..5844622hg19UCSC Ensembl
Outerchr19:5830681..5845122hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3813442
hg1913442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15984182
SamplesNA19663
Known GenesFUT3, FUT6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643541
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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