A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658100



Internal ID9924205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:88419076..88430923hg38UCSC Ensembl
Outerchr3:88419033..88430975hg38UCSC Ensembl
Innerchr3:88468226..88480073hg19UCSC Ensembl
Outerchr3:88468183..88480125hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3811943
hg1911943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv869e199
Supporting Variantsessv6316869, essv5656603, essv6497838, essv6114696
SamplesHG00537, HG00684, NA19003, NA18562
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658100
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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