A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6466110



Internal ID9320757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:63816863..63818174hg38UCSC Ensembl
Outerchr3:63816706..63818327hg38UCSC Ensembl
Innerchr3:63802539..63803850hg19UCSC Ensembl
Outerchr3:63802382..63804003hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381622
hg191622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2664605
Supporting Variants
SamplesNA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6466110
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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