A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596432



Internal ID6983747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66057699..66072607hg38UCSC Ensembl
Innerchr3:66057699..66072607hg38UCSC Ensembl
Outerchr3:66057199..66073107hg38UCSC Ensembl
chr3:66043374..66058282hg19UCSC Ensembl
Innerchr3:66043374..66058282hg19UCSC Ensembl
Outerchr3:66042874..66058782hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3814909
hg1914909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11030375
SamplesHG04035
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596432
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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