A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598071



Internal ID6985207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145541630..145560416hg38UCSC Ensembl
Innerchr3:145541780..145560266hg38UCSC Ensembl
Outerchr3:145541480..145560566hg38UCSC Ensembl
chr3:145259417..145278203hg19UCSC Ensembl
Innerchr3:145259567..145278053hg19UCSC Ensembl
Outerchr3:145259267..145278353hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3818787
hg1918787
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11171226, essv11171227
SamplesHG02394, HG00339
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598071
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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