A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665362



Internal ID9584781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152312420..152313395hg38UCSC Ensembl
chr1:152284896..152285871hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38976
hg19976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6445438, essv6431350
SamplesNA18505, NA19213
Known GenesFLG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665362
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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