A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5400613



Internal ID9701791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160177660..160182082hg38UCSC Ensembl
chr3:159895447..159899869hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg384423
hg194423
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676986
Supporting Variants
SamplesNA19452
Known GenesIL12A-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5400613
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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