A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1019314



Internal ID12182440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17224418..17224418hg38UCSC Ensembl
chr22:17705308..17705308hg19UCSC Ensembl
chr22:16085308..16085308hg18UCSC Ensembl
Cytoband22q11.1
Allele length
AssemblyAllele length
hg38332
hg19332
hg18332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4001263
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1019314
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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