A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598313



Internal ID6985449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157519188..157529744hg38UCSC Ensembl
Innerchr3:157519231..157529701hg38UCSC Ensembl
Outerchr3:157519145..157529787hg38UCSC Ensembl
chr3:157236977..157247533hg19UCSC Ensembl
Innerchr3:157237020..157247490hg19UCSC Ensembl
Outerchr3:157236934..157247576hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3810557
hg1910557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11195027, essv11195026
SamplesHG04235, HG04080
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598313
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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