A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647182



Internal ID7033923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:15322177..15344328hg38UCSC Ensembl
Innerchr22:15322677..15343828hg38UCSC Ensembl
Outerchr22:15321177..15345328hg38UCSC Ensembl
chr22:16633635..16655786hg19UCSC Ensembl
Innerchr22:16634135..16655286hg19UCSC Ensembl
Outerchr22:16632635..16656786hg19UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg3822152
hg1922152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16348118, essv16348117
SamplesHG03679, HG03695
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647182
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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