A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5992120



Internal ID9104021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160962483..160968220hg38UCSC Ensembl
chr3:160680271..160686008hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385738
hg195738
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672481
Supporting Variants
SamplesHG01095
Known GenesPPM1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5992120
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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