A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5760069



Internal ID9189226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:16953845..16977406hg38UCSC Ensembl
Outerchr3:16953808..16977456hg38UCSC Ensembl
Innerchr3:16995337..17018898hg19UCSC Ensembl
Outerchr3:16995300..17018948hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3823649
hg1923649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2675677
Supporting Variants
SamplesHG01465
Known GenesPLCL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5760069
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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