A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6398291



Internal ID9375694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132229092..132231797hg38UCSC Ensembl
chr3:131947936..131950641hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382706
hg192706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664445
Supporting Variants
SamplesNA19373
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6398291
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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