A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5839578



Internal ID9911246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:171534137..171536247hg38UCSC Ensembl
chr3:171251926..171254036hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg382111
hg192111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664501
Supporting Variants
SamplesNA20807
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5839578
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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