A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6213059



Internal ID8945410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:76183304..76186910hg38UCSC Ensembl
chr2:76410430..76414036hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg383607
hg193607
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675878
Supporting Variants
SamplesHG00476
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6213059
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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