A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598667



Internal ID6985803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:172594723..172600241hg38UCSC Ensembl
Innerchr3:172594757..172600207hg38UCSC Ensembl
Outerchr3:172594689..172600275hg38UCSC Ensembl
chr3:172312513..172318031hg19UCSC Ensembl
Innerchr3:172312547..172317997hg19UCSC Ensembl
Outerchr3:172312479..172318065hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg385519
hg195519
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11227329
SamplesHG01813
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598667
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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