A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675597



Internal ID9595016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:37165596..37166134hg38UCSC Ensembl
Outerchr3:37165559..37166184hg38UCSC Ensembl
Innerchr3:37207087..37207625hg19UCSC Ensembl
Outerchr3:37207050..37207675hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38626
hg19626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6526191
SamplesHG00123
Known GenesLRRFIP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675597
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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