A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662491



Internal ID9581910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77289716..77296046hg38UCSC Ensembl
chr3:77338867..77345197hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg386331
hg196331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6229037
SamplesHG01052
Known GenesROBO2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662491
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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