A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596886



Internal ID6984200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87374979..87379957hg38UCSC Ensembl
Innerchr3:87375129..87379807hg38UCSC Ensembl
Outerchr3:87374829..87380107hg38UCSC Ensembl
chr3:87424129..87429107hg19UCSC Ensembl
Innerchr3:87424279..87428957hg19UCSC Ensembl
Outerchr3:87423979..87429257hg19UCSC Ensembl
Cytoband3p11.2
Allele length
AssemblyAllele length
hg384979
hg194979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11063991, essv11063993, essv11063992
SamplesHG01149, HG01383, HG01269
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596886
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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