A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6157423



Internal ID8820803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:219889290..219895615hg38UCSC Ensembl
chr2:220754011..220760336hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg386326
hg196326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677981
Supporting Variants
SamplesHG00262
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6157423
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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