A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597691



Internal ID6984829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127085034..127105974hg38UCSC Ensembl
Innerchr3:127085534..127105474hg38UCSC Ensembl
Outerchr3:127084034..127106974hg38UCSC Ensembl
chr3:126803877..126824817hg19UCSC Ensembl
Innerchr3:126804377..126824317hg19UCSC Ensembl
Outerchr3:126802877..126825817hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3820941
hg1920941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11133241
SamplesHG03069
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597691
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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