A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598055



Internal ID6985191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145090891..145177304hg38UCSC Ensembl
Innerchr3:145090901..145177295hg38UCSC Ensembl
Outerchr3:145090882..145177314hg38UCSC Ensembl
chr3:144808665..144895091hg19UCSC Ensembl
Innerchr3:144808675..144895082hg19UCSC Ensembl
Outerchr3:144808656..144895101hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3886414
hg1986427
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv944e214
Supporting Variantsessv11169094, essv11169096, essv11169095
SamplesHG03172, HG02317, HG00339
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598055
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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