A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658467



Internal ID9577886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:111073839..111077472hg38UCSC Ensembl
Outerchr3:111073802..111077522hg38UCSC Ensembl
Innerchr3:110792686..110796319hg19UCSC Ensembl
Outerchr3:110792649..110796369hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg383721
hg193721
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5437059
SamplesHG01465
Known GenesPVRL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658467
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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