A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5632855



Internal ID9469400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:88860919..89267999hg38UCSC Ensembl
chr2:89160431..89567756hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38407081
hg19407326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666258
Supporting Variants
SamplesNA18940
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5632855
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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