A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664605



Internal ID9930710
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 StatusM
Merged Variants
Supporting Variantsessv6466110, essv5749696
SamplesNA19393, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664605
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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