A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598091



Internal ID6985227
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146292892..146363316hg38UCSC Ensembl
Innerchr3:146292957..146363251hg38UCSC Ensembl
Outerchr3:146292827..146363381hg38UCSC Ensembl
chr3:146010679..146081103hg19UCSC Ensembl
Innerchr3:146010744..146081038hg19UCSC Ensembl
Outerchr3:146010614..146081168hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3870425
hg1970425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11173070
SamplesHG02259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598091
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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