A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667475



Internal ID9933580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72510750..72518074hg38UCSC Ensembl
chr3:72559901..72567225hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg387325
hg197325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5681620, essv6153589
SamplesHG00501, HG00512
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667475
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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