A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637650



Internal ID7024441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3070074..3082577hg38UCSC Ensembl
chr16:3120075..3132578hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3812504
hg1912504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv474e214
Supporting Variantsessv15362856, essv15362858, essv15362859, essv15362855, essv15362861, essv15362857, essv15362860, essv15362854
SamplesHG01965, NA20808, NA12748, HG01512, HG01589, HG01342, NA20510, NA19074
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637650
Frequency
Sample Size2504
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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