A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5563213



Internal ID9436598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:32981272..32981609hg38UCSC Ensembl
Outerchr3:32981235..32981659hg38UCSC Ensembl
Innerchr3:33022764..33023101hg19UCSC Ensembl
Outerchr3:33022727..33023151hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38425
hg19425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659622
Supporting Variants
SamplesNA18636
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5563213
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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