A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595965



Internal ID6983283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:41114434..41119946hg38UCSC Ensembl
Innerchr3:41114434..41119946hg38UCSC Ensembl
Outerchr3:41114415..41119950hg38UCSC Ensembl
chr3:41155925..41161437hg19UCSC Ensembl
Innerchr3:41155925..41161437hg19UCSC Ensembl
Outerchr3:41155906..41161441hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg385513
hg195513
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10989679
SamplesNA19390
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595965
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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