A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595600



Internal ID6982918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25227233..25241301hg38UCSC Ensembl
Innerchr3:25227283..25241251hg38UCSC Ensembl
Outerchr3:25227156..25241378hg38UCSC Ensembl
chr3:25268724..25282792hg19UCSC Ensembl
Innerchr3:25268774..25282742hg19UCSC Ensembl
Outerchr3:25268647..25282869hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3814069
hg1914069
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10953001
SamplesNA21137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595600
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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