A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667549



Internal ID9933654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172868912..172876412hg38UCSC Ensembl
Outerchr3:172868851..172876482hg38UCSC Ensembl
Innerchr3:172586702..172594202hg19UCSC Ensembl
Outerchr3:172586641..172594272hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg387632
hg197632
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5653862, essv5535243
SamplesNA20808, HG00250
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667549
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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