A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635776



Internal ID7022574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22095526..22146218hg38UCSC Ensembl
chr15:22383477..22434169hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3850693
hg1950693
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15161540, essv15161539, essv15161537, essv15161538, essv15161541
SamplesHG01522, HG01177, HG01311, HG01512, HG01921
Known GenesOR4N3P, OR4N4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635776
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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