A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662107



Internal ID9928212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195434925..195435318hg38UCSC Ensembl
chr3:195155654..195156047hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38394
hg19394
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6240131, essv5794344, essv5584757, essv5793728, essv6100456
SamplesNA19383, NA19372, NA19982, NA18858, NA19102
Known GenesACAP2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662107
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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