A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665695



Internal ID9931800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85834814..85862731hg38UCSC Ensembl
chr6:86544532..86572449hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3827918
hg1927918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6387894, essv5989434, essv6420349, essv5505797, essv5909412, essv5968094
SamplesNA19819, NA19446, NA18519, NA19908, NA19835, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665695
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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