A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16394888



Internal ID6633931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:25307110..25388958hg38UCSC Ensembl
chr22:25703077..25784925hg19UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3881849
hg1981849
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3647458
Supporting Variants
SamplesNA20796
Known GenesIGLL3P, LRP5L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16394888
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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