A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5396021



Internal ID8373424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109919665..109920392hg38UCSC Ensembl
chr1:110462287..110463014hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38728
hg19728
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658285
Supporting Variants
SamplesHG00282
Known GenesCSF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5396021
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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