A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598222



Internal ID6985358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153281486..153325254hg38UCSC Ensembl
Innerchr3:153281486..153325254hg38UCSC Ensembl
Outerchr3:153280986..153325754hg38UCSC Ensembl
chr3:152999275..153043043hg19UCSC Ensembl
Innerchr3:152999275..153043043hg19UCSC Ensembl
Outerchr3:152998775..153043543hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3843769
hg1943769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11189808
SamplesNA19314
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598222
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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