A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662153



Internal ID9928258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:5706924..5707156hg38UCSC Ensembl
chr1:5766984..5767216hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38233
hg19233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6036122, essv5689657, essv6320453
SamplesNA19399, NA20340, NA19372
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662153
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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