A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668898



Internal ID9588317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24880559..24882161hg38UCSC Ensembl
chr2:25103428..25105030hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6568848, essv6222716
SamplesNA19461, NA19428
Known GenesADCY3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668898
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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