A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5645879



Internal ID9810846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:58548239..58551445hg38UCSC Ensembl
Outerchr3:58547868..58551815hg38UCSC Ensembl
Innerchr3:58533966..58537172hg19UCSC Ensembl
Outerchr3:58533595..58537542hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg383948
hg193948
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666180
Supporting Variants
SamplesNA19916
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5645879
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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