A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647313



Internal ID6687368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21101670..21110592hg38UCSC Ensembl
chr22:21455959..21464881hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg388923
hg198923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16370927, essv16370926, essv16370925
SamplesNA19210, HG03473, HG02013
Known GenesBCRP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647313
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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